@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI> .
@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/v4.0.0/void/> .

dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_head {
  this: np:hasAssertion dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_assertion;
    np:hasProvenance dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_provenance;
    np:hasPublicationInfo dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_assertion a np:Assertion .
  
  dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_provenance a np:Provenance .
  
  dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_assertion {
  miriam-gene:3292 a ncit:C16612 .
  
  lld:C0741682 a ncit:C7057 .
  
  dgn-gda:DGN545fe584a4cd8cf247b0306054dd900f sio:SIO_000628 miriam-gene:3292, lld:C0741682;
    a sio:SIO_001121 .
}

dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_provenance {
  dgn-np:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_assertion dcterms:description
      "[In addition, African American-predominant CYP1B1 432 Val allele was significantly more often found in the cases than in the controls overall and the HSD17B1 312 Gly allele was specifically associated with premenopausal breast cancer risk (OR=3.00, 95%CI 1.29-6.99).]. 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:19679043;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP757410.RAF3XbfwAtTKwhjMbSxB-eMv6iYQJip8_kVmSXlv6U-RI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:28+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}