@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc> .
@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:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_head {
  this: np:hasAssertion dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_assertion;
    np:hasProvenance dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_provenance;
    np:hasPublicationInfo dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_assertion a np:Assertion .
  
  dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_provenance a np:Provenance .
  
  dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN410ed9533337c330bea99b078e36fb4a sio:SIO_000628 miriam-gene:672, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_provenance {
  dgn-np:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_assertion dcterms:description
      "[Approximately 7%-10% of ovarian cancers occur in women with hereditary susceptibility, primarily secondary to mutations in BRCA1 and BRCA2, with smaller contributions from mutations in mismatch repair genes associated with the hereditary nonpolyposis colorectal cancer and other, as yet undiscovered, genes.]. 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:14530500;
    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:NP415977.RAZGIW4SYbnGCZXiWDe0cz4Fo93o58K4WTJzC8eNU38tc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:53+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" .
}