@prefix biocontext: <https://bioregistry.io/metaregistry/biocontext/> .
@prefix bioregistry: <https://bioregistry.io/registry/> .
@prefix bioregistry.metaresource: <https://bioregistry.io/metaregistry/> .
@prefix bioregistry.schema: <https://bioregistry.io/schema/#> .
@prefix dcat: <http://www.w3.org/ns/dcat#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix foaf: <http://xmlns.com/foaf/0.1/> .
@prefix miriam: <https://registry.identifiers.org/registry/> .
@prefix n2t: <https://bioregistry.io/metaregistry/n2t/resolve/> .
@prefix orcid: <https://orcid.org/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

bioregistry.metaresource:biocontext dcterms:hasPart biocontext:GWASCENTRAL.PHENOTYPE .

bioregistry.metaresource:bioregistry dcterms:hasPart bioregistry:gwascentral.phenotype .

bioregistry.metaresource:miriam dcterms:hasPart miriam:gwascentral.phenotype .

bioregistry.metaresource:n2t dcterms:hasPart n2t:gwascentral.phenotype .

bioregistry:gwascentral.phenotype a bioregistry.schema:0000001 ;
    rdfs:label "GWAS Central Phenotype" ;
    dcterms:description "GWAS Central (previously the Human Genome Variation database of Genotype-to-Phenotype information) is a database of summary level findings from genetic association studies, both large and small. It gathers datasets from public domain projects, and accepts direct data submission. It is based upon Marker information encompassing SNP and variant information from public databases, to which allele and genotype frequency data, and genetic association findings are additionally added. A Study (most generic level) contains one or more Experiments, one or more Sample Panels of test subjects, and one or more Phenotypes. This collection references a GWAS Central Phenotype."^^xsd:string ;
    dcterms:isPartOf bioregistry.metaresource:bioregistry ;
    skos:exactMatch biocontext:GWASCENTRAL.PHENOTYPE,
        n2t:gwascentral.phenotype,
        miriam:gwascentral.phenotype ;
    dcat:keyword "condition",
        "disease",
        "phenotype",
        "symptom" ;
    foaf:homepage <https://www.gwascentral.org/phenotypes> ;
    bioregistry.schema:0000005 "HGVPM623"^^xsd:string ;
    bioregistry.schema:0000006 "https://www.gwascentral.org/phenotype/$1"^^xsd:string ;
    bioregistry.schema:0000008 "^HGVPM\\d+$"^^xsd:string ;
    bioregistry.schema:0000012 false ;
    bioregistry.schema:0000019 orcid:0000-0002-0292-7972 ;
    bioregistry.schema:0000024 "https://www.gwascentral.org/phenotype/"^^xsd:string ;
    bioregistry.schema:0000027 <https://www.gwascentral.org/phenotype/HGVPM623> ;
    bioregistry.schema:0000029 "gwascentral.phenotype" .

orcid:0000-0002-0292-7972 rdfs:label "Tim Beck" ;
    foaf:mbox "tb143@leicester.ac.uk" .

biocontext:GWASCENTRAL.PHENOTYPE dcterms:isPartOf bioregistry.metaresource:biocontext .

n2t:gwascentral.phenotype dcterms:isPartOf bioregistry.metaresource:n2t .

miriam:gwascentral.phenotype dcterms:isPartOf bioregistry.metaresource:miriam .

