@prefix adms: <http://www.w3.org/ns/adms#> .
@prefix dcat: <http://www.w3.org/ns/dcat#> .
@prefix dcatap: <http://data.europa.eu/r5r/> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix foaf: <http://xmlns.com/foaf/0.1/> .
@prefix healthdcatap: <http://healthdataportal.eu/ns/health#> .
@prefix hydra: <http://www.w3.org/ns/hydra/core#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix vcard: <http://www.w3.org/2006/vcard/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

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    foaf:name "Wilhelmina Children's Hospital" .

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<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Olaf&lastName=Cremer&resource=MARS%20-%20Molecular%20Diagnosis%20and%20Risk%20Stratification%20of%20Sepsis> a vcard:Kind ;
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<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=ALL10> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "778"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
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    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=pmc&resource=ALL10> ;
    dct:description ""@en,
        """The aim of Protocol ALL-10 is to improve the overall treatment results in terms of EFS and to decrease
treatment intensity in patients with a pEFS of >95%. Therapy will be tailored according to the risk of
relapse as determined by the MRD levels at 2 time points during the first months of therapy. This
tailored therapy should lead to less intensive therapy for patients with low risk of relapse and to
intensification of therapy for patients with medium and high risk of relapse."""@nl ;
    dct:identifier <https://doi.org/10.71739/jr71-6h42> ;
    dct:issued "2026-02-25T07:45:46.145024"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:33:50.271121"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                """The aim of Protocol ALL-10 is to improve the overall treatment results in terms of EFS and to decrease
treatment intensity in patients with a pEFS of >95%. Therapy will be tailored according to the risk of
relapse as determined by the MRD levels at 2 time points during the first months of therapy. This
tailored therapy should lead to less intensive therapy for patients with low risk of relapse and to
intensification of therapy for patients with medium and high risk of relapse."""@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=pmc&resource=ALL10> ;
    dct:spatial <http://publications.europa.eu/resource/authority/country/NLD> ;
    dct:title ""@en,
        "Protocol ALL 10, protocol voor diagnostiek en behandeling van kinderen en adolescenten (1-19 jaar) met Acute Lymfatische Leukemie (ALL)"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Hester&lastName=de%20Groot-Kruseman&resource=ALL10> ;
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    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=ALL11> a dcat:Dataset ;
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    healthdcatap:numberOfUniqueIndividuals "887"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=PMC&resource=ALL11> ;
    dct:description ""@en,
        "1. To improve the overall outcome as compared to the previous protocols of the DCOG, especially ALL-9 and ALL-10. This is aimed for by decreasing therapy for part of the patients (TEL/AML1, Down syndrome, PPR only), increasing therapy for IKZF1 mutated cases, decreasing the cumulative dose of anthracyclines, omitting cranial irradiation and total body irradiation and individualizing asparaginase therapy for all patients. 2. Does a continuous schedule of Asparaginase lead to less allergic reaction/inactivation of Asparaginase than the standard non continuous schedule of Asparaginase? Patients are randomized to receive noncontinuous PEGasparaginase in IA (induction) and intensification of the Medium Risk group (standard arm A) or to receive continuous PEGasparaginase in IA, IB, M and intensification (continuous arm B) with the same cumulative number of doses of PEGasparaginase. 3. Does prophylactic administration of intravenous immunoglobulins reduce the number of infections during the intensive treatment phases? Patients are randomized in the induction and MR treatment group to receive or not receive prophylactic immunoglobulins. 4. Individualize the dose schedule of asparaginase by therapeutic drug monitoring in order to detect silent inactivation of asparaginase, to prevent allergic/anaphylactic reactions, to switch Asparaginase preparation in time and to prevent too high levels with possible toxicity."@nl ;
    dct:identifier <https://doi.org/10.71739/qmkv-2895> ;
    dct:issued "2026-02-25T07:46:00.765121"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:17.223403"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "1. To improve the overall outcome as compared to the previous protocols of the DCOG, especially ALL-9 and ALL-10. This is aimed for by decreasing therapy for part of the patients (TEL/AML1, Down syndrome, PPR only), increasing therapy for IKZF1 mutated cases, decreasing the cumulative dose of anthracyclines, omitting cranial irradiation and total body irradiation and individualizing asparaginase therapy for all patients. 2. Does a continuous schedule of Asparaginase lead to less allergic reaction/inactivation of Asparaginase than the standard non continuous schedule of Asparaginase? Patients are randomized to receive noncontinuous PEGasparaginase in IA (induction) and intensification of the Medium Risk group (standard arm A) or to receive continuous PEGasparaginase in IA, IB, M and intensification (continuous arm B) with the same cumulative number of doses of PEGasparaginase. 3. Does prophylactic administration of intravenous immunoglobulins reduce the number of infections during the intensive treatment phases? Patients are randomized in the induction and MR treatment group to receive or not receive prophylactic immunoglobulins. 4. Individualize the dose schedule of asparaginase by therapeutic drug monitoring in order to detect silent inactivation of asparaginase, to prevent allergic/anaphylactic reactions, to switch Asparaginase preparation in time and to prevent too high levels with possible toxicity."@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=PMC&resource=ALL11> ;
    dct:spatial <http://publications.europa.eu/resource/authority/country/NLD> ;
    dct:title ""@en,
        "PROTOCOL ALL 11: Treatment study protocol of the Dutch Childhood Oncology Group for Children and adolescents (1-19 year) with newly diagnosed acute lymphoblastic leukemia"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Hester&lastName=de%20Groot-Kruseman&resource=ALL11> ;
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    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

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    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMC%20Utrecht&resource=Athero-Express> ;
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        """The Athero-Express Biobank Study (AE) and the Abdominal Aortic Aneurysm-Express Biobank Study (AAA) are two ongoing, prospective biobank studies initiated in 2002 and 2003, respectively. Together, they comprise detailed histological and clinical data from over 4,500 patients who underwent arterial surgery at two Dutch tertiary referral centers.

The AE Biobank includes over 3,500 patients who underwent endarterectomy to remove atherosclerotic plaques, predominantly from the carotid and femoral arteries. The AAA Biobank includes over 1,000 patients who underwent open surgical repair of arterial aneurysms, primarily abdominal aortic aneurysms.

For both studies, blood and vascular tissue (plaque or aneurysm wall) were collected during surgery and stored at −80℃. Tissue material is routinely processed for standardised (immuno)histochemical analysis, with histological observations performed by the same dedicated technician, ensuring consistency; interobserver analyses have been previously reported.

In AE, the following plaque characteristics were quantified or scored:
	•	Macrophages (CD68) and smooth muscle cells (α-actin) as the percentage of field area using computerised analysis.
	•	Intraplaque vessel density (CD34) as the average count per 3 hotspots.
	•	Intraplaque haemorrhage (IPH) was scored as absent/present using hematoxylin and eosin (HE).
	•	Intraplaque fat was defined as < or ≥40% of total plaque area (HE).
	•	Calcification (HE) and collagen content (picrosirius red) were scored as no/minor vs. moderate/heavy staining.
	•	Overall plaque vulnerability was assessed following the method by Verhoeven et al.

In AAA, tissue sections were stained using:
	•	HE, EVG (elastin), picrosirius red (collagen), SMA (smooth muscle cells), CD68 (macrophages), CD3 (T cells), CD20 (B cells), CD138 (plasma cells), and von Willebrand factor (vasa vasorum).
	•	Each marker was semiquantitatively scored from 0 to 3 (0: none, 1: minor, 2: moderate, 3: heavy), separately for the intima, media, and adventitia, across both structural components and immune cell types.

For both cohorts, clinical data is obtained through standardised questionnaires, and supplemented with electronic health records where necessary.

Ethical approval for this study (TME/C-01.18) was provided by the Medical Research Ethics Committee of University Medical Center Utrecht, Utrecht, The Netherlands on 10 April 2002, and all research was conducted according to the principles of the Declaration of Helsinki (59th amendment, Seoul 2008) and in accordance with the Dutch Medical Research Involving Human Subjects Act (WMO)."""@nl ;
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    dct:modified "2026-05-13T11:34:41.457992"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "The Athero-Express Biobank Study (AE) is a longitudinal cross-sectional biobank study collecting blood and atherosclerotic plaque samples from patients undergoing endarterectomy. Clinical data is collected through standardised questionnaires and supplemented by querying electronic health records when needed. Patients are followed up to 3 years after surgery."@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMC%20Utrecht&resource=Athero-Express> ;
    dct:spatial <http://publications.europa.eu/resource/authority/country/NLD> ;
    dct:title ""@en,
        "Athero- and Aneurysm-Express Biobank Studies"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Sander&lastName=van%20der%20Laan&resource=Athero-Express> ;
    dcat:keyword "aneurysm"@nl,
        "arterial endarterectomy"@nl,
        "atherosclerosis"@nl,
        "plaque"@nl ;
    dcat:landingPage <http://www.atheroexpress.nl> ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=BioDay> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "2295"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:accrualPeriodicity <http://publications.europa.eu/resource/authority/frequency/AS_NEEDED> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Antonius&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Bravis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Catharina%20Ziekenhuis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Diakonessenhuis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=HagaZiekenhuis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=IJsselland%20Ziekenhuis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Isala%20Ziekenhuis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=MUMC&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Meander&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Medisch%20Centrum%20Leeuwarden&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Nij%20Smellinghe&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Radboudumc&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Spaarne%20Gasthuis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=St.%20Antonius%20Ziekenhuis&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Tergooi&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Tjongerschans&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCG&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=WKZ&resource=BioDay>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=ZorgSaam&resource=BioDay> ;
    dct:description ""@en,
        "The BioDay registry is a disease or condition registry for atopic dermatitis (AD)/prurigo nodularis (PN). All patients treated with advanced systemic therapy (biologics and JAK inhibitors [JAKi]) for AD are eligible for inclusion in the prospective, multicenter, observational BioDay registry. Patients are treated in a daily practice setting and the choice of treatment is determined by shared decision making and according to the Dutch AD guidelines. During all visits both clinical outcomes (e.g. EASI, IGA) and patient reported outcomes (e.g. NRS itch, DLQI,ADCT/RECAP) are collected."@nl ;
    dct:identifier <https://doi.org/10.71739/feb4-qv18> ;
    dct:issued "2026-02-25T07:45:50.884274"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:00.048651"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "Multicenter prospective observational atopic dermatitis registry"@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=BioDay> ;
    dct:spatial <http://catalogue.hdsu.nl/CatalogueOntologies/api/rdf/Regions/name=Friesland> ;
    dct:title ""@en,
        "BioDay Registry"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=BioDay&lastName=ContactEmail&resource=BioDay> ;
    dcat:keyword "JAK inhibitors"@nl,
        "abrocitinib"@nl,
        "atopic comorbidities"@nl,
        "atopic dermatitis"@nl,
        "baricitinib"@nl,
        "biologicals"@nl,
        "daily practice"@nl,
        "dupilumab"@nl,
        "lebrikizumab"@nl,
        "multicenter"@nl,
        "prurigo nodularis"@nl,
        "real-world evidence"@nl,
        "registry"@nl,
        "tralokinumab"@nl,
        "upadacitinib"@nl ;
    dcat:landingPage <http://bioday.nl> ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=EPIC-NL> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "40010"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:accrualPeriodicity <http://publications.europa.eu/resource/authority/frequency/OTHER> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=RIVM&resource=EPIC-NL>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=EPIC-NL> ;
    dct:description ""@en,
        """EPIC is the European Prospective Investigation Into Cancer and Nutrition.
EPIC-NL is the Dutch contribution to EPIC and comprises about 40,000 individuals prospectively followed since the early 90's. Biological samples have been stored in liquid nitrogen and repeated follow-up of the cohort has occured to obtain detailed information on lifestyle and behavioural factors and morbidity and mortality."""@nl ;
    dct:identifier <https://doi.org/10.71739/wfnj-cj15> ;
    dct:issued "2026-02-25T07:46:11.464809"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:25.569340"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                """At baseline, the prevalence of risk factors for chronic diseases was determined using self-administered questionnaires and a physical examination.
Participants are followed up over time for changes in exposure and for the occurrence of cancer, diabetes, cardiovascular diseases, and other medical conditions. Subgroups of participants were invited for several follow-up rounds."""@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=EPIC-NL> ;
    dct:spatial <http://catalogue.hdsu.nl/CatalogueOntologies/api/rdf/Regions/name=Limburg> ;
    dct:title ""@en,
        "European Prospective Investigation Into Cancer and Nutrition in the Netherlands (EPIC-NL)"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=EPIC-NL&lastName=Study%20team&resource=EPIC-NL> ;
    dcat:keyword "bloodsamples"@nl,
        "cancer"@nl,
        "cardiovascular disease"@nl,
        "cause of death"@nl,
        "chronic disease"@nl,
        "diabetes"@nl,
        "environmental exposure"@nl,
        "lifestyle"@nl,
        "morbidity"@nl,
        "mortality"@nl,
        "nutrition"@nl ;
    dcat:landingPage <https://epic.iarc.fr/centres/the-netherlands/> ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=HEM-PRO> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "192"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:accrualPeriodicity <http://publications.europa.eu/resource/authority/frequency/NEVER> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU%20-%20VCK&resource=HEM-PRO> ;
    dct:description ""@en,
        "In this single center retrospective cohort study, regular care data of total knee arthroplasty and total hip arthroplasty was extracted from medical records of people with bleeding disorders who attended the Van Creveldkliniek, University Medical Center Utrecht, between 1989 and 2025. Patients with moderate or severe haemophilia A or B (FVIII/FIX <5%) or Von Willebrand’s disease (VWD) with a FVIII activity <5% were included. All types of primary THA or TKA were included. All patients were followed according to standard care. The primary outcome was time to prosthesis failure, defined as revision or indication for revision (but patients are inoperable or refuse), measured in years."@nl ;
    dct:identifier <https://doi.org/10.71739/gp7d-fx35> ;
    dct:issued "2026-05-13T09:31:29.106246"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:05.820407"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "Single center retrospective cohort study,"@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU%20-%20VCK&resource=HEM-PRO> ;
    dct:spatial <http://publications.europa.eu/resource/authority/country/NLD> ;
    dct:title ""@en,
        "Long-term prosthesis survival of total hip and total knee arthroplasty in people with inherited bleeding disorders"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Gijs&lastName=Aertssen&resource=HEM-PRO> ;
    dcat:keyword "haemophilia"@nl,
        "joint arthroplasty"@nl,
        "survival"@nl,
        "total hip"@nl,
        "total knee"@nl ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=Julius%20Huisartsen%20Netwerk> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "1500000"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:accrualPeriodicity <http://publications.europa.eu/resource/authority/frequency/CONT> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=Julius%20Huisartsen%20Netwerk> ;
    dct:description ""@en,
        "The Julius General Practitioners Network (JHN) is a database of primary care routine data. It is a network of approximately seventy general practices with two hundred general practitioners and over 450,000 active patients in the Utrecht area. The database contains data on more than 1.5 million patients from 1995 to the present."@nl ;
    dct:identifier <https://doi.org/10.71739/r5zx-8143> ;
    dct:issued "2026-05-13T09:31:28.341150"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:33:55.781908"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "Electronic Health Recors of Patients in Primary Care"@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=Julius%20Huisartsen%20Netwerk> ;
    dct:spatial <http://catalogue.hdsu.nl/CatalogueOntologies/api/rdf/Regions/name=Utrecht> ;
    dct:title ""@en,
        "Julius Huisartsen Netwerk"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Secretariaat&lastName=JHN&resource=Julius%20Huisartsen%20Netwerk> ;
    dcat:keyword "Electronic Health Record"@nl,
        "General Practitioner"@nl,
        "Primary Care"@nl ;
    dcat:landingPage <https://www.juliushuisartsennetwerk.nl> ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=MARS%20-%20Molecular%20Diagnosis%20and%20Risk%20Stratification%20of%20Sepsis> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "17000"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:accrualPeriodicity <http://publications.europa.eu/resource/authority/frequency/NEVER> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=AMC&resource=MARS%20-%20Molecular%20Diagnosis%20and%20Risk%20Stratification%20of%20Sepsis>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=MARS%20-%20Molecular%20Diagnosis%20and%20Risk%20Stratification%20of%20Sepsis> ;
    dct:description ""@en,
        """MARS is a multicenter prospective cohort of ICU patients aimed at developing new molecular technologies for early diagnosis and risk stratification of sepsis.
MARS contains comprehensive clinical data (including admission diagnoses, comorbidities, daily treatments, medications, vital-signs, labs, and microbiology results). In addition, daily prospective adjudication of infection plausibility was performed, according to standardized definitions."""@nl ;
    dct:identifier <https://doi.org/10.71739/y3wf-hw15> ;
    dct:issued "2026-02-25T07:46:18.310427"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:29.959842"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "Ongoing prospective cohort and biobank of ICU patients admitted to the UMC Utrecht since 2011. The AMC was a participating center between 2011 and 2013."@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=MARS%20-%20Molecular%20Diagnosis%20and%20Risk%20Stratification%20of%20Sepsis> ;
    dct:spatial <http://catalogue.hdsu.nl/CatalogueOntologies/api/rdf/Regions/name=Noord-Holland> ;
    dct:title ""@en,
        "MARS - Molecular Diagnosis and Risk Stratification of Sepsis"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Olaf&lastName=Cremer&resource=MARS%20-%20Molecular%20Diagnosis%20and%20Risk%20Stratification%20of%20Sepsis> ;
    dcat:keyword "Biobank"@nl,
        "Biomarkers"@nl,
        "Blood samples"@nl,
        "Citrate"@nl,
        "Clinical"@nl,
        "Cohort"@nl,
        "EDTA"@nl,
        "Heparin"@nl,
        "ICU"@nl,
        "Infections"@nl,
        "Intensive Care"@nl,
        "Pathogen detection"@nl,
        "Plasma"@nl,
        "Pneumonia"@nl,
        "Prospective"@nl,
        "Vital signs"@nl ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=The%20TWIN-study> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "138"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMC%20Utrecht&resource=The%20TWIN-study> ;
    dct:description ""@en,
        """Inflammatory Bowel Diseases (IBD), i.e. Crohn’s Disease (CD) and Ulcerative
Colitis (UC), are thought to arise in genetically susceptible individuals in the context of
environmental triggers, with a potential dominant role for the interplay between the gut
microbiota, and the mucosal immune system. However, the relative importance and the
exact role of these factors in the pathogenesis of IBD is presently unknown. Interpretation of
published research in this field is often hampered by reverse causation, and data generated
in animal models cannot be directly extrapolated to the human condition. The disease is
probably triggered years before the occurrence of symptoms, but currently patients are only
identified when clinical disease is established. The preclinical phase of IBD might hold the
key to understanding the pathogenesis of IBD and could provide a huge window of
opportunity of halting or even preventing disease development. At this time, data on this
phase of the disease are limited. Identifying and validating biomarkers and
pathophysiological mechanisms is one of the necessary steps toward prediction, prevention
and optimalization of therapy in IBD care. Unaffected twin-siblings of IBD affected individuals
are at increased risk of developing IBD. Therefore, studying IBD-discordant, IBD-concordant
and non-IBD-concordant twins or multiples gives the unique opportunity to 1) define
mechanisms that underlie (the early development of) IBD and 2) identify and validate
markers of (pre)clinical IBD."""@nl ;
    dct:identifier <https://doi.org/10.71739/1fg4-jf23> ;
    dct:issued "2026-02-25T07:46:05.603630"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:21.966743"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "Observational study with both a cross-sectional and longitudinal design"@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMC%20Utrecht&resource=The%20TWIN-study> ;
    dct:spatial <http://publications.europa.eu/resource/authority/country/BEL> ;
    dct:title ""@en,
        "Twin cohort for the study of (pre)clinical Inflammatory Bowel Disease in the Netherlands: The TWIN-study"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Sarah%20Luna&lastName=Dijkstra&resource=The%20TWIN-study> ;
    dcat:keyword "Crohn s disease"@nl,
        "cohort"@nl,
        "concordance"@nl,
        "ibd"@nl,
        "twin"@nl,
        "twins"@nl,
        "ulcerative colitis"@nl ;
    dcat:landingPage <https://www.umcutrecht.nl/nl/wetenschappelijk-onderzoek/de-twin-studie-onderzoek-met-tweelingen-naar-chronische-ontstekingsziekten-van-de-darm-ibd> ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=UMBRELLA> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "7700"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:accrualPeriodicity <http://publications.europa.eu/resource/authority/frequency/AS_NEEDED> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Alrijne%20Ziekenhuis%20Leiderdorp&resource=UMBRELLA>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMC%20Utrecht&resource=UMBRELLA>,
        <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=Ziekenhuis%20Groep%20Twente&resource=UMBRELLA> ;
    dct:description ""@en,
        """The prospective, multicenter ‘Utrecht cohort for Multiple BREast cancer intervention studies and Long-term evaluAtion’ (UMBRELLA) cohort, established in 2013, serves as an infrastructure for conducting randomized controlled trials to evaluate effectiveness of (innovative) cancer treatments and survivorship care for breast cancer patients and survivors. UMBRELLA includes patients with histologically proven invasive breast cancer or ductal carcinoma in situ (DCIS) referred for breast cancer treatment in multiple hospitals in the Netherlands.

All UMBRELLA cohort participants consent for the collection and use of their clinical data. In addition, cohort participants can also provide consent for the longitudinal collection and use of patient-reported outcomes up to 10 years after enrolment. Last, cohort participants are also asked to provide consent to be randomized into future cohort-based trials following the Trial within Cohorts design. When conducting a cohort-based trial, all UMBRELLA cohort participants are screened for eligibility. Cohort participants assigned to the intervention arm, are offered the intervention, whereas cohort participants assigned to the control arm are not informed about the intervention and remain unaware of the trial.

By combining clinical data with (long-term) patient-reported outcomes from a large prospective cohort of breast cancer patients and survivors, it is possible to effectively study a diversity of clinically relevant questions to gain further insights in the effects of breast cancer treatment and its impact on quality of life as well as to evaluate effectiveness of interventions within the breast cancer field."""@nl ;
    dct:identifier <https://doi.org/10.71739/wd5m-j766> ;
    dct:issued "2026-02-25T07:46:24.123839"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:35.521115"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                "All UMBRELLA cohort participants consent for the collection and use of their clinical data. In addition, cohort participants can also provide consent for the longitudinal collection and use of patient-reported outcomes up to 10 years after enrolment. Last, cohort participants are also asked to provide consent to be randomized into future cohort-based trials following the Trial within Cohorts design. When conducting a cohort-based trial, all UMBRELLA cohort participants are screened for eligibility. Cohort participants assigned to the intervention arm, are offered the intervention, whereas cohort participants assigned to the control arm are not informed about the intervention and remain unaware of the trial."@nl ] ;
    dct:publisher <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMC%20Utrecht&resource=UMBRELLA> ;
    dct:spatial <http://catalogue.hdsu.nl/CatalogueOntologies/api/rdf/Regions/name=Zuid-Holland> ;
    dct:title ""@en,
        "'Utrecht cohort for Multiple BReast cancer intErvention studies and Long-term evaluation' cohort"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Contacts/firstName=Sofie&lastName=Gernaat&resource=UMBRELLA> ;
    dcat:keyword "Breast cancer  prospective cohort  multicenter  quality of life"@nl ;
    dcat:landingPage <https://www.umcutrecht.nl/nl/wetenschappelijk-onderzoek/umbrella> ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Resources/id=VIOOL> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2022/868/oj> ;
    healthdcatap:numberOfUniqueIndividuals "228"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:accrualPeriodicity <http://publications.europa.eu/resource/authority/frequency/NEVER> ;
    dct:creator <http://catalogue.hdsu.nl/catalogue-rdf/api/rdf/Agents/id=UMCU&resource=VIOOL> ;
    dct:description ""@en,
        "The VIOOL study is a prospective observational cohort conducted across three winter seasons (2021–2024; October–April/May) in the Netherlands. Children under 4 years of age were recruited from the community and followed for 16 weeks. Parents recorded daily symptom diaries and collected weekly nasal swabs, regardless of symptoms. Swabs were analyzed by PCR for a broad panel of common respiratory viruses. Its primary objective is to examine interactions between respiratory virus infections in young children. The study was approved by the Medical Ethics Committee of the University Medical Centre Utrecht (UMCU) and registered in the Clinical Trials Register (NL78424.041.21)."@nl ;
    dct:identifier <https://doi.org/10.71739/bbh4-yk15> ;
    dct:issued "2026-02-25T07:45:56.285550"^^xsd:dateTime ;
    dct:modified "2026-05-13T11:34:10.954441"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
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<https://fdp.healthdataspace.amsterdam/dataset/34eefc22-d313-4766-9f40-5fad618eb90d> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:creator [ a foaf:Agent ;
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            vcard:hasEmail <mailto:rdm@amsterdamumc.nl> ;
            foaf:homepage <https://www.amsterdamumc.nl/nl.htm> ;
            foaf:name "Amsterdam UMC" ] ;
    dct:description ""@en,
        "Data collection of the ABOARD Cohort started in 2022 and is ongoing. Participants receive annual online questionnaires on (mental) health, quality of life, and use of healthcare resources. In addition, medical data is collected from participants that visited a physician because of (self-reported) memory problems."@nl ;
    dct:identifier "AUMC-ABOARD-D1" ;
    dct:issued "2026-03-12T08:16:58.935311"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
    dct:modified "2026-05-13T11:33:03.791136"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                ""@nl ] ;
    dct:publisher [ a foaf:Agent ;
            dct:identifier <https://ror.org/05grdyy37> ;
            vcard:hasEmail <mailto:rdm@amsterdamumc.nl> ;
            foaf:homepage <https://www.amsterdamumc.nl/nl.htm> ;
            foaf:name "Amsterdam UMC" ] ;
    dct:title ""@en,
        "ABOARD Cohort"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint [ a vcard:Kind ;
            vcard:fn "ABOARD Cohort" ;
            vcard:hasEmail <mailto:aboard-cohort@amsterdamumc.nl> ] ;
    dcat:keyword "Alzheimer"@nl,
        "Dementia"@nl,
        "PROMS"@nl ;
    dcat:qualifiedAttribution [ a dcat:Attribution ;
            dcat:agent [ a foaf:Agent,
                        foaf:Organization ;
                    dct:identifier "0000-0001-8766-6224" ;
                    foaf:homepage <https://orcid.org/0000-0001-8766-6224> ;
                    foaf:mbox <mailto:alzheimercentrum@amsterdamumc.nl> ;
                    foaf:name "Wiesje van der Flier" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<https://fdp.healthdataspace.amsterdam/dataset/3cff6c7d-823d-45ef-bba3-f5abe3c2c27a> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:creator [ a foaf:Agent ;
            dct:identifier <https://ror.org/03xqtf034> ;
            vcard:hasEmail <mailto:repository@nki.nl> ;
            foaf:homepage <https://ror.org/03xqtf034> ;
            foaf:name "Nederlands Kanker Instituut - Antoni van Leeuwenhoekziekenhuis" ] ;
    dct:description ""@en,
        "Background The faecal immunochemical test (FIT) is widely employed for colorectal cancer screening. However, its sensitivity for advanced precursor lesions remains suboptimal. The multitarget FIT (mtFIT), measuring haemoglobin, calprotectin, and serpin family F member 2, has demonstrated enhanced sensitivity for advanced neoplasia, especially advanced adenomas, at equal specificity to FIT. This study aimed to prospectively validate and investigate the clinical utlitity of mtFIT versus FIT in a setting of population-based colorectal cancer screening.  Methods Individuals aged 55–75 years and who were eligible for the Dutch national FIT-based colorectal cancer screening programme were invited to submit both a FIT and mtFIT sample collected from the same bowel movement. Positive FIT (47 μg/g haemoglobin cutoff) or mtFIT (based on decision-tree algorithm) led to a colonoscopy referral. The primary outcome was the relative detection rate of mtFIT versus FIT for all advanced neoplasia. Secondary outcomes were the relative detection rates of colorectal cancer, advanced adenoma, and advanced serrated polyps individually and the long-term effect of mtFIT-based versus FIT-based programmatic screening on colorectal cancer incidence, mortality, and cost, determined with microsimulation modelling. The study has been registered in ClinicalTrials.gov, NCT05314309, and is complete.  Findings Between March 25 and Dec 7, 2022, 35786 individuals were invited to participate in the study, of whom 15283 (42·7%) consented, and 13187 (86·3%) of 15283 provided both mtFIT and FIT samples with valid results. Of the 13187 participants, 6637 (50·3%) were male and 6550 (49·7%) were female. mtFIT showed a 9·11% (95% CI 8·62–9·61) positivity rate and 2·27% (95% CI 2·02–2·54) detection rate for advanced neoplasia, compared with a positivity rate of 4·08% (3·75–4·43) and a detection rate of 1·21% (1·03–1·41) for FIT. Detection rates of mtFIT versus FIT were 0·20% (95% CI 0·13–0·29) versus 0·17% (0·11–0·27) for colorectal cancer; 1·64% (1·43–1·87) versus 0·86% (0·72–1·04) for advanced adenoma, and 0·43% (0·33–0·56) versus 0·17% (0·11–0·26) for advanced serrated polyps. Modelling demonstrated that mtFIT-based screening could reduce colorectal cancer incidence by 21% and associated mortality by 18% compared with the current Dutch colorectal cancer screening programme, at feasible costs. Furthermore, at equal positivity rates, mtFIT outperformed FIT in terms of diagnostic yield. At an equally low positivity rate, mtFIT-based screening was predicted to further decrease colorectal cancer incidence by 5% and associated mortality by 4% compared with FIT-based screening.  Interpretation The higher detection rate of mtFIT for advanced adenoma compared with FIT holds the potential to translate into additional and clinically meaningful long-term colorectal cancer incidence and associated mortality reductions in programmatic colorectal cancer screening.  Funding Stand Up to Cancer, Dutch Cancer Society, Dutch Digestive Foundation, and Health~Holland."@nl ;
    dct:identifier <https://doi.org/10.1016/S1470-2045%2823%2900651-4> ;
    dct:issued "2026-03-12T08:16:43.481229"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
    dct:modified "2026-05-13T11:33:11.976938"^^xsd:dateTime ;
    dct:provenance [ a dct:ProvenanceStatement ;
            rdfs:label ""@en,
                ""@nl ] ;
    dct:publisher [ a foaf:Agent ;
            dct:identifier <https://ror.org/03xqtf034> ;
            vcard:hasEmail <mailto:repository@nki.nl> ;
            foaf:homepage <https://ror.org/03xqtf034> ;
            foaf:name "Nederlands Kanker Instituut - Antoni van Leeuwenhoekziekenhuis" ] ;
    dct:title ""@en,
        "The multitarget faecal immunochemical test for improving stool-based colorectal cancer screening programmes: a Dutch population-based, paired-design, intervention study"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint [ a vcard:Kind ;
            vcard:fn "Gerrit Meijer" ;
            vcard:hasEmail <mailto:g.meijer@nki.nl> ] ;
    dcat:distribution <https://fdp.healthdataspace.amsterdam/distribution/bb9f1071-7380-4276-95bb-861edc35bdb2>,
        <https://fdp.healthdataspace.amsterdam/distribution/dd0daf50-6672-491d-b44e-dc5bd2dc01be> ;
    dcat:keyword "Adenoma"@nl,
        "Colorectal Neoplasms"@nl,
        "Defecation"@nl,
        "Early Detection of Cancer"@nl,
        "Hemoglobins"@nl,
        "Humans"@nl ;
    dcat:qualifiedAttribution [ a dcat:Attribution ;
            dcat:agent [ a foaf:Agent,
                        foaf:Organization ;
                    dct:identifier "https://www.nki.nl/research/find-a-researcher/groupleaders/gerrit-meijer/" ;
                    foaf:homepage <https://orcid.org/0000-0003-0330-3130> ;
                    foaf:mbox <mailto:g.meijer@nki.nl> ;
                    foaf:name "Gerrit Meijer" ] ],
        [ a dcat:Attribution ;
            dcat:agent [ a foaf:Agent,
                        foaf:Organization ;
                    dct:identifier "https://www.amc.nl/web/research-75/person-1/prof.-dr.-e.-dekker.htm" ;
                    foaf:homepage <https://orcid.org/0000-0002-4363-0745> ;
                    foaf:mbox <mailto:e.dekker@amsterdamumc.nl> ;
                    foaf:name "Evelien Dekker" ] ],
        [ a dcat:Attribution ;
            dcat:agent [ a foaf:Agent,
                        foaf:Organization ;
                    dct:identifier "https://www.erasmusmc.nl/en/research/researchers/spaander-mcw" ;
                    foaf:homepage <https://orcid.org/0000-0002-9103-9757> ;
                    foaf:mbox <mailto:v.spaander@erasmusmc.nl> ;
                    foaf:name "Manon Spaander" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<https://fdp.healthdataspace.amsterdam/dataset/4103e594-893d-487a-a939-00aa3fe1f0eb> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
    dct:creator [ a foaf:Agent ;
            dct:identifier <https://ror.org/03xqtf034> ;
            vcard:hasEmail <mailto:repository@nki.nl> ;
            foaf:homepage <https://www.nki.nl/> ;
            foaf:name "Nederlands Kanker Instituut - Antoni van Leeuwenhoekziekenhuis" ] ;
    dct:description ""@en,
        "Purpose: Circulating tumor DNA (ctDNA) has the potential to guide therapy selection and monitor treatment response in patients with metastatic cancer. However, germline and clonal hematopoiesis–associated alterations can confound identification of tumor-specific mutations in cell-free DNA (cfDNA), often requiring additional sequencing of tumor tissue. The current study assessed whether ctDNA-based treatment response monitoring could be performed in a tumor tissue–independent manner by combining ultra-deep targeted sequencing analyses of cfDNA with patient-matched white blood cell (WBC)-derived DNA.  Experimental Design: In total, 183 cfDNA and 49 WBC samples, along with 28 tissue samples, from 52 patients with metastatic colorectal cancer participating in the prospective phase III CAIRO5 clinical trial were analyzed using an ultra-deep targeted sequencing liquid biopsy assay.  Results: The combined cfDNA and WBC analysis prevented false-positives due to germline or hematopoietic variants in 40% of patients. Patient-matched tumor tissue sequencing did not provide additional information. Longitudinal analyses of ctDNA were more predictive of overall survival than standard-of-care radiological response evaluation. ctDNA mutations related to primary or acquired resistance to panitumumab were identified in 42% of patients.  Conclusions: Accurate calling of ctDNA mutations for treatment response monitoring is feasible in a tumor tissue–independent manner by combined cfDNA and patient-matched WBC genomic DNA analysis. This tissue biopsy-independent approach simplifies sample logistics and facilitates the application of liquid biopsy ctDNA testing for evaluation of emerging therapy resistance, opening new avenues for early adaptation of treatment regimens."@nl ;
    dct:identifier <https://doi.org/10.1158/1078-0432.CCR-22-2538> ;
    dct:issued "2026-03-12T08:16:41.394031"^^xsd:dateTime ;
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    dct:modified "2026-05-13T11:33:44.884268"^^xsd:dateTime ;
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            rdfs:label ""@en,
                ""@nl ] ;
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            foaf:homepage <https://www.nki.nl/> ;
            foaf:name "Nederlands Kanker Instituut - Antoni van Leeuwenhoekziekenhuis" ] ;
    dct:title ""@en,
        "Metastatic Colorectal Cancer Treatment Response Evaluation by Ultra-Deep Sequencing of Cell-Free DNA and Matched White Blood Cells"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint [ a vcard:Kind ;
            vcard:fn "Nederlands Kanker Instituut - Antoni van Leeuwenhoekziekenhuis" ;
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        <https://fdp.healthdataspace.amsterdam/distribution/e60d91e8-85f9-4c95-891a-4555a0d227a1> ;
    dcat:keyword "Cell-Free Nucleic Acids"@nl,
        "Circulating Tumor DNA"@nl,
        "Colonic Neoplasms"@nl,
        "High-Throughput Nucleotide Sequencing"@nl,
        "Humans"@nl,
        "Mutation"@nl,
        "Neoplasm DNA"@nl,
        "Prospective Studies"@nl,
        "Rectal Neoplasms"@nl,
        "Tumor Biomarkers"@nl ;
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                    dct:identifier "https://orcid.org/0000-0003-2076-5521" ;
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                    foaf:mbox <mailto:r.fijneman@nki.nl> ;
                    foaf:name "Remond J.A. Fijneman" ] ;
            dcat:hadRole <https://standards.iso.org/iso/19115/resources/Codelists/gml/CI_RoleCode.xml#principalInvestigator> ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<https://fdp.healthdataspace.amsterdam/dataset/8aeecb41-90ab-4044-88bf-28b5c21d9a67> a dcat:Dataset ;
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    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
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            vcard:hasEmail <mailto:rdm@amsterdamumc.nl> ;
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            foaf:name "Amsterdam UMC" ] ;
    dct:description ""@en,
        "Data collection of the Amsterdam Dementia Cohort started in 2010 and is ongoing. All study participants undergo a standardized screening protocol for dementia. This dataset includes data on neuroimaging-and neurophysiology data including MRI, EEG, and MEG."@nl ;
    dct:identifier "AUMC-ADC-D3" ;
    dct:issued "2026-03-12T08:16:54.538506"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
    dct:modified "2026-05-13T11:33:24.980345"^^xsd:dateTime ;
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                ""@nl ] ;
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            foaf:homepage <https://www.amsterdamumc.nl/nl.htm> ;
            foaf:name "Amsterdam UMC" ] ;
    dct:title ""@en,
        "Amsterdam Dementia Cohort - Neuroimaging & Neurophysiology "@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
    dcat:contactPoint [ a vcard:Kind ;
            vcard:fn "Amsterdam Dementia Cohort" ;
            vcard:hasEmail <mailto:databaseteamADC@amsterdamumc.nl> ] ;
    dcat:inSeries <https://ckan.healthdata.nl/dataset/b58f5004-dc3e-4206-85c1-96ce0aaf8b03> ;
    dcat:keyword "Alzheimer"@nl,
        "Dementia"@nl,
        "EEG"@nl,
        "Imaging"@nl,
        "MEG"@nl,
        "MRI"@nl,
        "Neurophysiology"@nl ;
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                    foaf:mbox <mailto:alzheimercentrum@amsterdamumc.nl> ;
                    foaf:name "Wiesje van der Flier" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

<https://fdp.healthdataspace.amsterdam/dataset/c5f2b92f-1900-4a7c-a3f4-e7bbe3904323> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    healthdcatap:numberOfRecords "232929"^^xsd:nonNegativeInteger ;
    healthdcatap:numberOfUniqueIndividuals "10460"^^xsd:nonNegativeInteger ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/NON_PUBLIC> ;
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            vcard:hasEmail <mailto:biobank@amsterdamumc.nl> ;
            foaf:homepage <https://www.amsterdamumc.nl/nl.htm> ;
            foaf:name "Amsterdam UMC" ] ;
    dct:description ""@en,
        "The Amsterdam Dementia Cohort was established in 2000, along with the foundation of the VU University Medical Center (VUmc) Alzheimer Center in the Netherlands. All patients that visit the Alzheimer Center are asked to consent to the use of their clinical data for scientific purposes. This population of patients comprises the Amsterdam Dementia Cohort, which consisted of almost 8,000 patients as of the 1st of January, 2021. After a baseline visit, the majority of patients visit the clinic annually for follow-up."@nl ;
    dct:identifier "VB21-0021" ;
    dct:issued "2026-03-12T08:16:38.931577"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
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            dcat:endDate "2017-01-01T01:00:00+00:00"^^xsd:dateTime ] ;
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        ""@nl ;
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            vcard:fn "Amsterdam UMC Biobank" ;
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        "Biobank"@nl,
        "Dementia"@nl,
        "Samples"@nl ;
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                    foaf:name "Wiesje van der Flier" ] ] ;
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            foaf:name "Amsterdam UMC" ] ;
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        "Data collection of the Amsterdam Dementia Cohort started in 2010 and is ongoing. All study participants undergo a standardized screening protocol for dementia. This dataset includes data on demographics and neurological-and physical examination."@nl ;
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    dct:issued "2026-03-12T08:16:52.942342"^^xsd:dateTime ;
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            foaf:name "Amsterdam UMC" ] ;
    dct:title ""@en,
        "Amsterdam Dementia Cohort - Demographics & Neurological/Physical Examination"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
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            vcard:fn "Amsterdam Dementia Cohort" ;
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        "Dementia"@nl,
        "Demographics"@nl ;
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                    foaf:name "Wiesje van der Flier" ] ;
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        ""@nl ;
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    dct:title ""@en,
        "Health-RI cBioPortal: CAIRO5 (Clinical Cancer Res 2023)"@nl ;
    dcat:accessURL <https://cbioportal.health-ri.nl/study/summary?id=CAIRO5_CLINCANCERRES2023> ;
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    dct:description ""@en,
        ""@nl ;
    dct:format <https://publications.europa.eu/resource/authority/file-type/TAR_GZ> ;
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        <https://definities.geostandaarden.nl/dcat-ap-nl/id/waardelijst/licenties/naamsvermelding_niet_commercieel_gelijk_delen40> ;
    dct:title ""@en,
        "EGA: Tissue DNA, WBC DNA and cfDNA (deep-)sequencing of mCRC patients treated with doublet chemotherapy and anti-EGFR in the CAIRO5 study."@nl ;
    dcat:accessURL <https://ega-archive.org/studies/EGAS00001006695> ;
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                    foaf:homepage <https://nhr.nl/> ;
                    foaf:mbox <mailto:wetenschap@nhr.nl> ;
                    foaf:name "Nederlandse Hart Registratie" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> ;
    foaf:page <https://nhr.nl/wetenschappelijk-onderzoek/> .

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    healthdcatap:populationCoverage "collection type: Other | data categories: Not available | materials: Other | omics: Proteomics | imaging: N | sex: Not asked"@nl ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "DCVA sample collection Outflow tract related aging with congenital heart defects: identifying causes and mechanisms of myocardial and large vessel wall adaptation, predictors for long term outcome and targets for improved treatment."@nl ;
    dct:identifier "DCVA-057" ;
    dct:issued "2021-10-01T00:00:00+00:00"^^xsd:dateTime ;
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                ""@nl ] ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
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            dcat:startDate "2021-10-01T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "Outflow tract related aging with congenital heart defects: identifying causes and mechanisms of myocardial and large vessel wall adaptation, predictors for long term outcome and targets for improved treatment."@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
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            vcard:fn "DCVA" ;
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        "Not available"@nl,
        "OUTREACH  WP6"@nl,
        "Other"@nl,
        "Proteomics"@nl ;
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                    foaf:mbox <mailto:info@dcvalliance.nl> ;
                    foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

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    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    healthdcatap:minTypicalAge "18"^^xsd:nonNegativeInteger ;
    healthdcatap:numberOfUniqueIndividuals "13800"^^xsd:nonNegativeInteger ;
    healthdcatap:populationCoverage "collection type: Cohort,Disease specific,Hospital | data categories: Medical records,National registries,Physiological/Biochemical measurements,Survey data | materials: Not available | omics: Not available | imaging: N | sex: Female,Male"@nl ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/RESTRICTED> ;
    dct:creator [ a foaf:Agent ;
            dct:identifier "DCVA" ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "CAPACITY is a registry of patients with COVID-19 across Europe and has been established to answer questions on the role of cardiovascular disease in this pandemic. It is an extension of the Case Record Form (CRF) that was released by the ISARIC (International Severe Acute Respiratory and Emerging Infection Consortium) and WHO (World Health Organisation) in response to the emerging outbreak of COVID-19.The aim of CAPACITY is to collect data regarding the cardiovascular history, diagnostic information and occurrence of cardiovascular complications in COVID-19 patients. By collecting this information in a standardized manner, CAPACITY can aid in providing more insight in (1) the incidence of cardiovascular complications in patients with COVID-19, and (2) the vulnerability and clinical course of COVID-19 in patients with an underlying cardiovascular disease"@nl ;
    dct:identifier "DCVA-058" ;
    dct:issued "2020-03-27T00:00:00+00:00"^^xsd:dateTime ;
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    dct:modified "2026-05-13T11:47:00.610951"^^xsd:dateTime ;
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            rdfs:label ""@en,
                ""@nl ] ;
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            dct:identifier "DCVA" ;
            vcard:hasEmail <mailto:info@dcvalliance.nl> ;
            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            dcat:endDate "2020-08-24T00:00:00+00:00"^^xsd:dateTime ;
            dcat:startDate "2020-03-27T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "CAPACITY-COVID"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
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            vcard:fn "DCVA" ;
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            vcard:hasURL <['https://www.dcvalliance.nl/']> ] ;
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        "Cohort"@nl,
        "Disease specific"@nl,
        "Female"@nl,
        "Hospital"@nl,
        "Male"@nl,
        "Medical records"@nl,
        "National registries"@nl,
        "Not available"@nl,
        "Physiological Biochemical measurements"@nl,
        "Survey data"@nl ;
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                    foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ] ;
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<https://fdp.heart-institute.nl/dataset/110d7de3-9f7d-46ff-9838-cbcc0ad1c577> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    healthdcatap:maxTypicalAge "85"^^xsd:nonNegativeInteger ;
    healthdcatap:minTypicalAge "42"^^xsd:nonNegativeInteger ;
    healthdcatap:populationCoverage "collection type: Cohort,Disease specific,Hospital,Non-Human,Sample collection | disease: Other conduction disorders | data categories: Biological samples,Imaging data,Medical records,Physiological/Biochemical measurements,Other | materials: cDNA / mRNA,Cell lines,DNA,Serum,Tissue, cryo preserved | omics: Proteomics | imaging: N | sex: Female,Male"@nl ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/RESTRICTED> ;
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            dct:identifier "DCVA" ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "Atrial fibrillation (AF) is the most common age-related cardiac rhythm disorder accounting for about one-third of rhythm abnormalities related hospitalizations with annual costs in the European Union of 13 billion euro. Early recognition of AF is essential for prevention of disease progression from recurrent intermittent episodes to finally permanent AF. This progression is accompanied by a gradual increase in therapy failure and can in the end-stage even with extensive therapy not be treated. Persistence of AF is rooted in the presence of electropathology, which is defined as complex electrical conduction disorders caused by structural damage of atrial tissue. Therefore, early recognition of AF susceptibility in patients is of prime importance to halt electropathology and hence disease onset and progression. At present, AF can only be diagnosed with a surface electrocardiogram when a patient already suffers from AF. In addition, this rhythm registration cannot assess the degree of electropathology and thus the stage of AF which is essential for selection of the appropriate therapy. Hence, early recognition of AF and the start of effective treatment is seriously hampered. By exploiting electropathology, we are able to develop a novel diagnostic instrument to predict AF onset and early progression. We hypothesize that every patient has a unique biological and electrical signal profile that is influenced by age, gender and heart disease. This bio-electrical profile is deduced from the ratio abnormal/normal electrical signals in the atria and determination of specific biomarkers levels in tissue or blood samples related to structural damage. These outcomes are summarized in an AF Fingerprint. The primary objective of this project is to design a patient-specific invasive and non-invasive AF Fingerprint, which reveals the degree of electropathology and can be used to early recognize AF onset or progression in daily clinical practice. Hereto we utilize a bottom-up study design consisting of 3 different phases; AF Fingerprinting during longstanding persistent AF, progression from recurrent intermittent to persistent AF and early recognition of AF onset in a broad population. In order to achieve this we aim to 1) develop signal processing algorithms for automatic assessment of electrical profiles by quantifying signal features, 2) establish the effects of patient characteristics, different stages of AF on invasive electrical signal profiles by utilizing a unique high density atrial mapping approach (golden standard measurements) during cardiac surgery and non-invasive electrical signal profiles consisting of whole-heart body surface electrocardiograms, 3) construct AF Fingerprints, by correlating electrical signal profiles with levels of specific biomarkers related to structural damage in atrial tissue (invasive AF Fingerprint) and blood-based biomarkers (non-invasive AF Fingerprint) 4) design a mapping device for signal acquisition, compatible with the developed algorithmic software, for general use in clinical practice, replacing current available prototypes restricted by a limited number of electrode positions. At the end of this project, AF Fingerprinting can be used in daily clinical practice for early recognition or progression of AF by determination of stage of electropathology. As such, AF Fingerprinting enables early and optimal patient tailored AF treatment, thereby improving patient's outcome."@nl ;
    dct:identifier "DCVA-022" ;
    dct:issued "2017-01-01T00:00:00+00:00"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
    dct:modified "2026-05-13T11:44:04.711357"^^xsd:dateTime ;
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            rdfs:label ""@en,
                ""@nl ] ;
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            dct:identifier "DCVA" ;
            vcard:hasEmail <mailto:info@dcvalliance.nl> ;
            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            dcat:startDate "2017-01-01T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "Atrial Fibrillation Fingerprinting"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
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            vcard:fn "DCVA" ;
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            vcard:hasURL <['https://www.dcvalliance.nl/']> ] ;
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        "Biological samples"@nl,
        "Cell lines"@nl,
        "Cohort"@nl,
        "DNA"@nl,
        "Disease specific"@nl,
        "Female"@nl,
        "Hospital"@nl,
        "Imaging data"@nl,
        "Male"@nl,
        "Medical records"@nl,
        "Non-Human"@nl,
        "Other"@nl,
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        "Physiological Biochemical measurements"@nl,
        "Proteomics"@nl,
        "Sample collection"@nl,
        "Serum"@nl,
        "Tissue"@nl,
        "cDNA   mRNA"@nl,
        "cryo preserved"@nl ;
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                    dct:identifier "DCVA" ;
                    foaf:homepage <https://www.dcvalliance.nl/> ;
                    foaf:mbox <mailto:info@dcvalliance.nl> ;
                    foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

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    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    healthdcatap:minTypicalAge "18"^^xsd:nonNegativeInteger ;
    healthdcatap:populationCoverage "collection type: Hospital | disease: coronary artery disease | data categories: Medical records,National registries,Survey data,Other | imaging: Y | sex: Undifferentiated"@nl ;
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            dct:identifier "DCVA" ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "CARRIER proposes a big data-driven approach to detection and prevention of coronary artery disease. Models learnt from big data will help identify patients at increased risk and will drive disease management. An electronic lifestyle coach will support adherence to a personalised health management plan co-created by patients and clinicians."@nl ;
    dct:identifier "DCVA-047" ;
    dct:issued "2020-01-01T00:00:00+00:00"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
    dct:modified "2026-05-13T11:46:09.383107"^^xsd:dateTime ;
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                ""@nl ] ;
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            dct:identifier "DCVA" ;
            vcard:hasEmail <mailto:info@dcvalliance.nl> ;
            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            dcat:endDate "2025-01-01T00:00:00+00:00"^^xsd:dateTime ;
            dcat:startDate "2020-01-01T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "Coronary ARtery disease: Risk estimations and Interventions for prevention and EaRly detection"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
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        "Hospital"@nl,
        "Medical records"@nl,
        "National registries"@nl,
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        "Undifferentiated"@nl,
        "coronary artery disease"@nl ;
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                    foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

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    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    healthdcatap:maxTypicalAge "70"^^xsd:nonNegativeInteger ;
    healthdcatap:minTypicalAge "27"^^xsd:nonNegativeInteger ;
    healthdcatap:numberOfUniqueIndividuals "220"^^xsd:nonNegativeInteger ;
    healthdcatap:populationCoverage "collection type: Cohort | disease: Other cerebrovascular diseases - Cerebral aneurysm, nonruptured | data categories: Imaging data,Medical records | materials: Not available | omics: Genomics | imaging: Y | sex: Female,Male"@nl ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/RESTRICTED> ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "ERASE will deliver: 1. Knowledge if we should also offer screening for intracranial aneurysms (IA) to persons 1. who have a positive family history with first degree relatives with unruptured IA and 2. ≥35 yr who smoke(d) and have hypertension. 3. Genetic, clinical and anatomical risk factors that will contribute to the ability to predict persons at risk for IAs."@nl ;
    dct:identifier "DCVA-018" ;
    dct:issued "2016-12-01T00:00:00+00:00"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
    dct:modified "2026-05-13T11:47:05.956845"^^xsd:dateTime ;
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            rdfs:label ""@en,
                ""@nl ] ;
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            dct:identifier "DCVA" ;
            vcard:hasEmail <mailto:info@dcvalliance.nl> ;
            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            dcat:endDate "2021-11-30T00:00:00+00:00"^^xsd:dateTime ;
            dcat:startDate "2016-12-01T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "Optimal Early Recognition of persons at high risk of Aneurysmal Subarachnoid hemorrhagE"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
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        "ERASE"@nl,
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        "Genomics"@nl,
        "Imaging data"@nl,
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        "Medical records"@nl,
        "Not available"@nl,
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    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

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    healthdcatap:populationCoverage "collection type: Population-based | data categories: Imaging data,Medical records,Physiological/Biochemical measurements,Other | materials: Not available | omics: Not available | imaging: Y | sex: Female,Male"@nl ;
    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/RESTRICTED> ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "Developing AI for ECG interpretation"@nl ;
    dct:identifier "DCVA-055" ;
    dct:issued "2018-11-01T00:00:00+00:00"^^xsd:dateTime ;
    dct:language <http://id.loc.gov/vocabulary/iso639-1/en> ;
    dct:modified "2026-05-13T11:45:52.980454"^^xsd:dateTime ;
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                ""@nl ] ;
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            dct:identifier "DCVA" ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
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            dcat:endDate "2032-11-30T00:00:00+00:00"^^xsd:dateTime ;
            dcat:startDate "2018-11-01T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "ECG-AI"@nl ;
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        ""@nl ;
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            vcard:fn "DCVA" ;
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            vcard:hasURL <['https://www.dcvalliance.nl/']> ] ;
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        "Female"@nl,
        "Imaging data"@nl,
        "Male"@nl,
        "Medical records"@nl,
        "Not available"@nl,
        "Other"@nl,
        "Physiological Biochemical measurements"@nl,
        "Population-based"@nl ;
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                    foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ] ;
    dcat:theme <http://publications.europa.eu/resource/authority/data-theme/HEAL> .

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    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
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    dct:accessRights <http://publications.europa.eu/resource/authority/access-right/RESTRICTED> ;
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            dct:identifier "DCVA" ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "DCVA sample collection Renal connection to microvascular disease and heart failure with preserved ejection fraction: the next phase"@nl ;
    dct:identifier "DCVA-066" ;
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                ""@nl ] ;
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    dct:title ""@en,
        "Renal connection to microvascular disease and heart failure with preserved ejection fraction: the next phase"@nl ;
    adms:versionNotes ""@en,
        ""@nl ;
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        "We collected cardiac data (history, phusica; examination, Echo, ECG, Blood) from 1550 chidlhood cancer survivors and 250 sibling."@nl ;
    dct:identifier "DCVA-029" ;
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        "Een gezonde leefstijl - een gezond voedingspatroon en voldoende bewegen - draagt in belangrijke mate bij aan de preventie van chronische ziekten. Mensen met lage sociaal-economische status (SES) hebben vaak een ongezondere leefstijl dan mensen met een hogere SES. Echter, interventies gericht op het stimuleren van een gezonde leefstijl bereiken juist deze lage SES doelgroep slecht en kunnen sociale ongelijkheid vergroten. Een mogelijke verklaring hiervoor is dat interventies zich traditioneel veelal richten op individuele determinanten van gedrag zoals kennis, attitudes en intenties. Bovendien zijn deze interventies veelal niet effectief, mede doordat er geen rekening gehouden wordt met de - sociale, fysieke en politieke - context waarin leefstijlkeuzes gemaakt worden: ongezond gedrag kan worden gezien als een automatische reactie op de 'obesogene' omgeving. Veranderingen in en van de omgeving waarin mensen leven kunnen in belangrijke mate helpen om een gezonde leefstijl te bevorderen en alle doelgroepen te bereiken. Door veranderingen in de omgeving moet gezorgd worden dat de gezonde keuze de makkelijke keuze, de voor de hand liggende keuze of zelfs de enige keuze wordt, juist ook voor de moeilijke bereikbare en veranderbare doelgroepen zoals mensen met een lagere opleiding. Echter, of omgevingsinterventies ook op langere termijn effectief zijn voor het verbeteren van risicofactoren voor hart- en vaatziekten is niet bekend en moet onderzocht worden. In SUPREME NUDGE wordt een geïntegreerde interventie in supermarkten ontwikkeld en onderzocht, waarin de 'supermarktomgeving' zo wordt ingericht dat de gezonde voedselkeuze makkelijker en vanzelfsprekender wordt. De supermarkt is een belangrijke omgeving waarin (leefstijl)keuzes worden gemaakt, en waar het verleiden tot gezondere voedingskeuzes via productplaatsing, prijsverandering en berichten directe en langdurende effecten kan hebben. Dit wordt gecombineerd met een m-health promotion interventie waarmee mensen direct en op maat feedback en adviezen krijgen over hoeveel ze waar en wanneer bewegen, en hoe ze meer kunnen gaan bewegen. De effecten op risicofactoren voor hart- en vaatzieken worden onderzocht. Deze interventie bouwt voort op eerdere effectieve interventies om gezonde voeding en voldoende beweging te bevorderen, maar combineert twee innovatieve benaderingen: 'nudging' en prijsverandering, met 'real-time' feedback waarbij gebruik wordt gemaakt van kunstmatige intelligentie en context-specifieke informatie en adviezen over leefstijlgedrag."@nl ;
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    dct:description ""@en,
        "A campaign to inform the general public and online tools to evaluate indications for cardiogenetic referral will be launched. The yield of novel methods to reach out to family members will be investigated and if successful, implemented into routine cascade testing. Advanced non-invasive imaging and non-invasive electrophysiological measurements will be performed in mutation carriers and asymptomatic family members to detect early signs of cardiac disease, with special attention to sex differences. As exemplar for all inherited cardiomyopathies, early detection at individual and cellular level will focus on patients and their family members with PLN or PKP2 gene founder mutations. Early detection facilitates risk stratification and timely therapeutic interventions, thereby reducing mortality and morbidity. A national infrastructure will be developed to facilitate biomarker discovery and follow-up research. Extensive genetic and phenotypic (including imaging) data will be stored and integrated into a central data warehouse to facilitate data sharing and guarantee long-term sustainability of the registries. As such, e-DETECT will help in the prevention of cardiac dysfunction and SCD among young, apparently healthy individuals. By 2030, the consortium aims to increase the uptake of cascade testing in family members by 50% and thereby detect up to 25% more patients at true risk. This increased uptake will enable regular follow up and timely treatment, thereby reducing morbidity and mortality."@nl ;
    dct:identifier "DCVA-016" ;
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        ""@nl ;
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        "The CAS study is a clinical observational study investigating the effects of ConAoS on the left   ventricular function and the prevalence, pattern and expanse of LVH, myocardial stiffness and   myocardial fibrosis. Moreover, we will assess the prognostic capacity of the presence of these   pathological processes, correlating our findings at baseline to clinical outcome by assessing the   occurrence of cardiovascular events and all-cause mortality during 3-year clinical follow-up. We will   unravel biomarker and imaging predictors for myocardial dysfunction (systolic and diastolic) with   specific attention for male-female differences"@nl ;
    dct:identifier "DCVA-059" ;
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        "Outflow tract related aging with congenital heart defects: identifying causes and mechanisms of myocardial and large vessel wall adaptation, predictors for long term outcome and targets for improved treatment."@nl ;
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    dct:description ""@en,
        "De Hartfalen registratie omvat patiënten met hartfalen die voldoen aan de richtlijnen en definitie ESC 2021 en 2023 focused update. De inclusie betreft in ieder geval de Novo HF patiënten met HFrEF, die primair voor hun hartfalen op de poli komen (+/- klinische opname vooraf) voor instellen van hun diagnose en behandeling van hartfalen. Voor de Hartfalen-registratie worden de patiënten tot 1 jaar na hun diagnose opgevolgd tenzij de patiënt eerder teruggaat naar de eerstelijn, overlijdt of wordt doorverwezen."@nl ;
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        "To optimally use brain imaging data in vascular cognitive impairment (VCI), the ImProVas project (i) develops and validates methods for automatic quantification of microbleeds and lacunar infarcts and (ii) develops and validates prediction methods utilizing these biomarkers. The project extends existing cohorts with novel image-derived biomarkers (HBC: https://www.ncbi.nlm.nih.gov/pubmed/29017156; TRACE-VCI: https://www.ncbi.nlm.nih.gov/pubmed/28428166)."@nl ;
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    dct:title ""@en,
        "Improved Prognosis of Vascular cognitive impairment using automatic quantitative imaging biomarker extraction and disease modeling"@nl ;
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        ""@nl ;
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	• transcatheter-mitralisklepingrepen
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	• plaatsing van plugs ten behoeve van paravalvulaire lekkage (PVL)-sluiting
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Hier geldt dat elke poging tot een ingreep wordt geïncludeerd vanaf het moment dat de patiënt is aangeprikt en/of een huidincisie heeft plaatsgevonden."""@nl ;
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            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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        ""@nl ;
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        "Inherited cardiomyopathies (CM) are clinically heterogeneous: age of onset and disease-severity differ greatly between patients with the exact same gene mutation. The mechanisms that underlie the variation in disease susceptibility are unknown.  Pilot data of DOSIS suggest an important role for secondary disease-modifiers such as additional (epi)genetic variations, environmental disease triggers, and an age-related decline in protein quality control (PQC). The PQC system prevents onset of CM by suppressing the accumulation of toxic proteins in cardiomyocytes. Moreover, CM severity is attenuated by the stimulation of protein degradation pathways. Thus, a healthy PQC system keeps mutant expression below the toxic dose. In addition, mutation location in a gene may determine disease susceptibility due to specific mutation-induced changes in protein structure, which alter PQC recognition, and affect incorporation into the sarcomere.  Hypothesis: the clinical variability in CM is determined by (1) interplay between (epi)genetic and ageing-induced environmental factors (burden); (2) status of the PQC system (coping mechanisms); (3) mutation location.  Aims:   1.	Identify (epi)genetic modifiers influencing the CM phenotype in individuals carrying a sarcomeric mutation.  2.	Elucidate derailment of the PQC system as determinant of cellular toxicity in CM.  3.	Establish the toxic effect of mutants with respect to protein dose and mutation location.  4.	Obtain proof of concept for age-dependent secondary disease-modifiers as key players in protein toxicity of CM mutations and test novel pharmacological interventions.  DOSIS is directed at understanding the path a mutation needs to travel to become toxic, and at testing novel therapies in experimental model systems."@nl ;
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        ""@nl ;
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    healthdcatap:populationCoverage "collection type: Disease specific,Image collection | disease: Cardiomyopathy - Endocardial fibroelastosis | data categories: Genealogical records,Imaging data,Other | materials: Not available | omics: Not available | imaging: Y | sex: Female,Male"@nl ;
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            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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        "Electrocardiographic imaging in patients to identify early signs of disease in arrhytmogenic cardiomyopathy. Therefore, clinical MRI/CT, body surface mapping (64-electrode ECG) and 3D imaging of the electrode positions is carried out."@nl ;
    dct:identifier "DCVA-017" ;
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    dct:title ""@en,
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        ""@nl ;
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    healthdcatap:populationCoverage "collection type: Hospital,Non-Human | disease: Atherosclerosis | data categories: Biological samples,Imaging data | materials: cDNA / mRNA,Peripheral blood cells,Plasma,RNA,Serum | omics: Genomics,Transcriptomics | imaging: N | sex: Female,Male"@nl ;
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        "GENIUS II"@nl ;
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        ""@nl ;
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        "Imaging data"@nl,
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    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
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    healthdcatap:populationCoverage "collection type: Hospital,Longitudinal,Sample collection,Other | disease: Pneumonia due to staphylococcus aureus | data categories: Physiological/Biochemical measurements | materials: Not available | omics: Not available | imaging: N | sex: Female,Male"@nl ;
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            dct:identifier "DCVA" ;
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    dct:description ""@en,
        "We investigated whether hyperaggregation occurs during infection, and whether aspirin inhibits this. Patients hospitalised due to acute infection were randomised to receive 10 days of aspirin treatment or no intervention. Our outcome measures were PFA-Closure Time, serum thromboxane and plasma thromboxane."@nl ;
    dct:identifier "DCVA-067" ;
    dct:isReferencedBy <https://doi.org/10.1007/s10238-023-01101-5>,
        <https://pubmed.ncbi.nlm.nih.gov/37294478/> ;
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        "The efficacy of aspirin to inhibit platelet aggregation in patients hospitalised with a severe infection: a multicentre, open‑label, randomised controlled trial"@nl ;
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        ""@nl ;
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    healthdcatap:numberOfUniqueIndividuals "30"^^xsd:nonNegativeInteger ;
    healthdcatap:populationCoverage "collection type: Case-Control,Disease specific,Longitudinal,Population-based | data categories: Imaging data,Medical records,Physiological/Biochemical measurements,Survey data | materials: Serum | omics: Not available | imaging: Y | sex: Female,Male"@nl ;
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            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "Rationale: Tetralogy of Fallot is the most common type of cyanotic congenital heart disease. The main problems of this patient population are heart failure related to chronic pulmonary regurgitation, arrhythmias and sudden cardiac death. A major gap in our knowledge is how coupling between the RV and pulmonary artery affects outcomes. It has been shown that aortic pulse wave velocity can be improved by exercise training in Tetralogy of Fallot.  Objective: Primary Objective: To examine the effect of an online based exercise training protocol on ventriculo-arterial coupling , as assessed by pulse wave velocity in the aorta and pulmonary artery in patients operated for  Tetralogy of Fallot.  Study design:  cross-over interventional study. All children and young adults will be randomized in 2 groups. One group will start with care/exercise as usual, the other group will start with an online exercise training. After 12 weeks the groups will change from protocol. Before start of measurements, after 12 weeks and group 2 after 24 weeks, all participants will undergo a number of tests, including echocardiogram, cardiopulmonary exercise test, and cardiac magnetic resonance imaging.   Study population: 12-30 years of age, after surgical repair of tetralogy of Fallot (TOF), being followed at one of the 2 locations of the Academic Center for Congenital Heart disease (ACAHA).  Intervention: 12 weeks of online based interval training 3 times a week.  Main study parameters/endpoints: Decrease in pulse wave velocity in the aorta and pulmonary artery measured by MRI."@nl ;
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            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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    dct:title ""@en,
        "Outflow tract related aging with congenital heart disease. Workpackage Tetraogy of fallot High Intensity Interval Training"@nl ;
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        ""@nl ;
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        "Disease specific"@nl,
        "Female"@nl,
        "Imaging data"@nl,
        "Longitudinal"@nl,
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        "Medical records"@nl,
        "Not available"@nl,
        "OUTREACH  ToFHIIT study"@nl,
        "Physiological Biochemical measurements"@nl,
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                    foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ] ;
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    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
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    healthdcatap:minTypicalAge "18"^^xsd:nonNegativeInteger ;
    healthdcatap:numberOfUniqueIndividuals "500"^^xsd:nonNegativeInteger ;
    healthdcatap:populationCoverage "collection type: Cohort,Disease specific,Hospital | data categories: Imaging data,Medical records,Physiological/Biochemical measurements,Survey data | materials: Not available | omics: Not available | imaging: Y | sex: Female,Male"@nl ;
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            dct:identifier "DCVA" ;
            vcard:hasEmail <mailto:info@dcvalliance.nl> ;
            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "With our project we strive to maximally utilize existing data and registries. However, new data needs to  be  collected,  primarily  due  to  three  reasons:  (1)  routine  clinical  care  so  far  has  lacked  standardized diagnostic tests for the detection of myocardial damageafter COVID-19; (2) the established cohorts have no funding for repeated measurements/follow-up to assess the (ir)reversibility of myocardial damage and (3) no patient reported outcome data are available that could function as a potential alert of ongoing myocardial problems following COVID-19."@nl ;
    dct:identifier "DCVA-061" ;
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                ""@nl ] ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            dcat:startDate "2017-12-15T00:00:00+00:00"^^xsd:dateTime ] ;
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        "REVIVING EARLY DIAGNOSIS OF CARDIOVASCULAR DISEASE"@nl ;
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        ""@nl ;
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        "Heart failure"@nl,
        "Longitudinal"@nl,
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        "RED-CVD"@nl,
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    dct:description ""@en,
        "De Cardiochirurgie registratie omvat uitgevoerde cardiochirurgische ingrepen aan het hart en/of de grote intrathoracale vaten, al dan niet in combinatie met een niet-cardiale ingreep. Een sessie beslaat de periode vanaf het moment van huidincisie of -punctie tot en met het verlaten van de operatiekamer of de ruimte waar de interventie heeft plaatsgevonden. Ook afgebroken interventies nadat er al een huidincisie of -punctie heeft plaatsgevonden vallen binnen een sessie zijn geïncludeerd."@nl ;
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        ""@nl ;
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        "CABG"@nl,
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        "MVP"@nl,
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        "aortic surgery"@nl,
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        "heart valve surgery"@nl,
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    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
    healthdcatap:populationCoverage "collection type: Disease specific,Image collection,Non-Human,Rare disease collection | disease: Primary pulmonary hypertension | data categories: Biological samples,Imaging data,Physiological/Biochemical measurements | materials: cDNA / mRNA,Cell lines,Peripheral blood cells,Plasma,RNA,Serum,Tissue, cryo preserved,Tissue, paraffin preserved,Whole Blood | omics: Transcriptomics | imaging: Y | sex: Female,Male"@nl ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "PAH is a deadly disease characterized by abnormal remodelling of pulmonary vessels, leading to a progressive increase in pulmonary artery pressure and right heart failure. PHAEDRA-IMPACT aims to prevent disease development by early identification of the patient at risk, and identification and treatment of treatable traits in different forms and stages of the disease."@nl ;
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                ""@nl ] ;
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            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            dcat:startDate "2019-04-01T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "Pulmonary Hypertension and AssociatED Right heart fAilure: IMproved outcomes through Precision medicine, Advanced modelling and early deteCTion"@nl ;
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        ""@nl ;
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    healthdcatap:populationCoverage "collection type: Other | disease: Atherosclerotic heart disease | data categories: Imaging data,Medical records | materials: Not available | omics: Not available | imaging: Y | sex: Female,Male"@nl ;
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    dct:description ""@en,
        "CONCRETE aims to evaluate whether GP access to CT calcium scoring leads to earlier CAD diagnosis and treatment. The design is a pragmatic cluster randomized trial in which direct access to CT calcium scoring is compared to routine clinical care in patients with chest discomfort. Randomization will take place at GP level. Patients in both clusters will be asked for consent to fill in questionnaires and for the researchers to gather data on work-up and follow-up."@nl ;
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                ""@nl ] ;
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    dct:title ""@en,
        "COroNary Calcium scoring as fiRst-linE Test to dEtect and exclude coronary artery disease in GP patients with stable chest pain"@nl ;
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        ""@nl ;
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    dct:description ""@en,
        "For this reason,  there is an urgent need for large prospective cohort studies in which patients with laboratory  confirmed COVID-19 unselectively undergo standardized and long-term follow-up to assess  the occurrence and natural history of cardiac abnormalities. In the current study, we aim to  determine if and how often (residual) cardiac damage can be detected in patients who have  recovered from COVID-19. Furthermore, we strive to gain additional insight into the etiology  in patients that develop (residual) damage of the heart."@nl ;
    dct:identifier "DCVA-062" ;
    dct:issued "2021-03-01T00:00:00+00:00"^^xsd:dateTime ;
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                ""@nl ] ;
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        "CAPACITY 2: A prospective cohort study evaluating the occurrence of short and long-term cardiac and cerebrovascular complications in patients hospitalized for COVID-19"@nl ;
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        ""@nl ;
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        "This project aims at investigating if the mechanism of trained immunity plays a role in the development of atherosclerosis in women with former preeclampsia."@nl ;
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                ""@nl ] ;
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        ""@nl ;
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<https://fdp.heart-institute.nl/dataset/8fefa40e-a2a0-4e1d-b300-fdf100674f5f> a dcat:Dataset ;
    dcatap:applicableLegislation <http://data.europa.eu/eli/reg/2025/327/oj> ;
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    healthdcatap:minTypicalAge "18"^^xsd:nonNegativeInteger ;
    healthdcatap:populationCoverage "collection type: Disease specific,Hospital,Image collection,Longitudinal,Non-Human,Rare disease collection | disease: Congenital insufficiency of aortic valve | data categories: Biological samples,Imaging data,Medical records | materials: DNA,Plasma,Serum | omics: Genomics | imaging: Y | sex: Female,Male"@nl ;
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            dct:identifier "DCVA" ;
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            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
    dct:description ""@en,
        "The bicuspid aortic valve is generally considered to be a result of a congenital fusion of two out of three leaflets. We found that the non-coronary leaflet develops from the same embryonic structure that also gives rise to the right coronary leaflet. A BAV type 2 can be considered as the result of an improper separation rather than an abnormal fusion of two separately developed leaflets, which is an essential different starting point for our research to explore the genetic and signalling pathways of BAV genesis. We also have found in a bicuspid aortic model (NOS3 knock out) that 2 out 3 contributing extracardiac cell populations (neural crest and second heart field) are disturbed in their contribution to both the aortic valvular leaflets and the aorta wall. This results in BAV and abnormal elastin production in the ascending aortic wall from its initial formation in the embryo onwards. Hemodynamics seems to play a more modest role in the formation of the aorta aneurysm than one has generally considered up till now. To study the role of haemodynamics in EMT during valve formation and calcification we made use of the ex vivo miniature tissue culture system. In cultured mouse adult hearts, we found that by changing flow, the response of valve endothelial cells is altered. By culturing valves of mice with a genetic endothelial lineage trace, we could show that when exposed to high physiological flow, the endothelial cell phenotype and lining is maintained. Interestingly, by adding calcification inducing factors such as B-glycerolphosphate, dexamethasone or Bone Morphogenetic Proteins, we were able to induce valvular calcification in the cultured adult mouse hearts. We further studied the role of haemodynamics in the pathology of BAV by immunoshistochemical analysis of aortic material. We observed that at the non-jet side of the aorta the endothelial cells showed a significantly increased inflammation (P50+), endothelial-to-mesenchymal-transition (SNAI1+) and trend towards increased proliferation in BAV patients. Our results show an increased endothelial activity at the inner curvature of the ascending aorta/aortic arch with oscillatory flow in BAV patients. In human aortic samples from BAV patients, we have identified that the protein FHL2 is increased in the dilated aorta compared with the non-dilated aorta. FHL2 is an interesting biomarker as it has been described to reduce smooth muscle cell contractility. Our observed increase in FHL2 expression in the dilated aorta could therefore be related to an increase in synthetic SMCs, causing the breakdown of the elastic lamellae and destabilization of the aorta. We investigated women with Turner syndrome using advanced imaging technology to study structural abnormalities. We focused on partial abnormal pulmonary venous return and found that 25% of the women indeed had this abnormality, a much higher prevalence than expected. In addition, we discovered structural abnormalities in the aortic arch, large arteries and coronary arteries. This last finding is completely new. We also investigated the aorta flow with 4D MRI in patients with BAV and demonstrated the feasibility of this technique to estimate regurgitation and showed good correlation with echocardiography. Of patients with coarctation, approximately 50% to 75% have a bicuspid aortic valve. We found that coarctation stent treatment in Turner patients is associated with a higher risk than normal. Finally, we investigated the risk of dissection and found a lower risk than expected. Aortic stenosis is the most frequent complication of bicuspid aortic valve and the main reason for valve surgery during lifetime. Different options for valve replacement are available and we investigated the outcomes for the different options in children and adults. Then an information portal was developed according to the systematic International Patient Decision Aid Standards (IPDAS) development process. First, we conducted comprehensive surveys and interviews among patients (N=63), caregivers of pediatric patients (N=10) and physicians (N=32) to assess the current state of patient information and explore their preferences and needs, to determine the focus for the development of the information portal. We found that patient knowledge and numeracy is limited, reliable information is scarce, physicians inform patients selectively and patient involvement is suboptimal. Then we tested the impact of the information portal on the subjective quality of life. We found no effect, however, when studying the results in more detail we found that 50% of the patients never visited the website and that in the patients who did visit the website there was a clear positive effect on the quality of life. We discovered a new gene mutation on SMAD6 in patients with a bicuspid aortic valve that is associated with aortic aneurysm. Also we discovered TBX20 as a contributing gene. Finally, loss-of-function mutations in the X-linked biglycan gene were found to cause a severe syndromic form of thoracic aortic aneurysms and dissections."@nl ;
    dct:identifier "DCVA-009" ;
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                ""@nl ] ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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            dcat:startDate "2016-06-01T00:00:00+00:00"^^xsd:dateTime ] ;
    dct:title ""@en,
        "DETECTIN-HF"@nl ;
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        ""@nl ;
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        "Digoxin Evaluation in Chronic heart failure: Investigational Study In Outpatients in the Netherlands"@nl ;
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        ""@nl ;
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        ""@nl ;
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        "This project explores continuous video monitoring of the cardiorespiratory status of a patient as an innovative unobtrusive method that could aid to reduce workload for the staff and better predict deterioration."@nl ;
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        ""@nl ;
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            foaf:name "Dutch Cardiovascular Alliance (DCVA)" ] ;
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        "Rationale: Whilst patients with a tetralogy of Fallot have excellent survival in the present  day, adverse events still occur regularly. However,risk stratification in these patients is not sufficient at this moment.  Objective: The objective of this study is to report the long-term follow-up after ToF repair  in a relatively large cohort and to determine  predictors of long-term adverse outcomes.  Study design: Retrospective observational study  Study population:  patients operated for tetralogy of Fallot in in the Netherlands  Intervention (if applicable): n/a  Main study parameters/endpoints: Cardiac related adverse events during the follow-up of  tetralogy of Fallot"@nl ;
    dct:identifier "DCVA-060" ;
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            foaf:homepage <https://www.dcvalliance.nl/> ;
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