@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_head {
  this: np:hasAssertion dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion;
    np:hasProvenance dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_provenance;
    np:hasPublicationInfo dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion a np:Assertion .
  
  dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_provenance a np:Provenance .
  
  dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion {
  miriam-gene:1586 a ncit:C16612 .
  
  lld:C0007103 a ncit:C7057 .
  
  dgn-gda:DGN39858cace7e037b9ef25be6b5a96b90b sio:SIO_000628 miriam-gene:1586, lld:C0007103;
    a sio:SIO_001122 .
}

dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_provenance {
  dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion dcterms:description
      "[The position -34T/C variant in CYP17A1 appears to be associated with reduced risk of endometrial cancer, with those homozygous for the variant allele having about half the risk of those homozygous for the wild type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:17110639;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:58+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}