@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_head {
  this: np:hasAssertion dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion;
    np:hasProvenance dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_provenance;
    np:hasPublicationInfo dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion a np:Assertion .
  
  dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_provenance a np:Provenance .
  
  dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1333600 a ncit:C7057 .
  
  dgn-gda:DGN63e54b0499ad9dc1146c3726d1fbfbb5 sio:SIO_000628 miriam-gene:672, lld:C1333600;
    a sio:SIO_001121 .
}

dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_provenance {
  dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion dcterms:description
      "[To estimate the proportion of ovarian cancers attributable to founding mutations in BRCA1 and BRCA2 in the Jewish population and the familial cancer risks associated with each, we interviewed 213 Jewish women with ovarian cancer at 11 medical centers in North America and Israel and offered these women genetic testing for the three founder mutations.]. 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:10739756;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}