@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU> .
@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:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_head {
  this: np:hasAssertion dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_assertion;
    np:hasProvenance dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_provenance;
    np:hasPublicationInfo dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_assertion a np:Assertion .
  
  dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_provenance a np:Provenance .
  
  dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGNeafdfb7c2d60feda5242dd097c0e0585 sio:SIO_000628 miriam-gene:675, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_provenance {
  dgn-np:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_assertion dcterms:description
      "[The identification of germ-line mutations in 2 genes (BRCA1 and BRCA2) responsible for the majority of hereditary ovarian cancers has led an increasing number of women carriers of these mutations to undergo prophylactic oophorectomy (PO) to reduce their risk of subsequent ovarian carcinoma.]. 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:17001151;
    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:NP571107.RAoc6qI61jtvTHSvsbm9N5zQn7nlHqRVMX0NC-pvWMuhU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:03+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" .
}