@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg> .
@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:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_head {
  this: np:hasAssertion dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_assertion;
    np:hasProvenance dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_provenance;
    np:hasPublicationInfo dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_assertion a np:Assertion .
  
  dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_provenance a np:Provenance .
  
  dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_assertion {
  miriam-gene:23038 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGN1ea1a93439cca2b073b3d92f807a3b5c sio:SIO_000628 miriam-gene:23038, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_provenance {
  dgn-np:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_assertion dcterms:description
      "[We believe that given the growing appreciation of the prognostic significance of BRCA mutations and the differential chemosensitivity shown by these tumors, as well as the potential of novel agents such as poly(ADP-ribose) polymerase inhibitors, the identification of a germline BRCA mutation concurrent with a new diagnosis of ovarian cancer will significantly impact on tailoring personalized ovarian management in the future.]. 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:20973257;
    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:NP773850.RAYXtbpxai5mw0-7Ys6C_0QTa7Zk7Rlaail_FA4wSF9Yg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:48+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" .
}