@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps> .
@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:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_head {
  this: np:hasAssertion dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_assertion;
    np:hasProvenance dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_provenance;
    np:hasPublicationInfo dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_assertion a np:Assertion .
  
  dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_provenance a np:Provenance .
  
  dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGNad31262295ea9db92acb5d88ca25583c sio:SIO_000628 miriam-gene:672, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_provenance {
  dgn-np:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_assertion dcterms:description
      "[Although BRCA1/2 mutation testing is not warranted in the general Finnish ovarian cancer patient population, patients who have also been diagnosed with breast cancer or have family history of breast or breast and ovarian cancer could benefit from referral to genetic counselling and mutation testing.]. 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:11436123;
    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:NP322709.RA5RoWBPJGWadsyQ19anH6ckIFZPhkJd_aaXQPDZY_Cps130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:11+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" .
}