@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_head { this: np:hasAssertion dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_assertion; np:hasProvenance dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_provenance; np:hasPublicationInfo dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_publicationInfo; a np:Nanopublication . dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_assertion a np:Assertion . dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_provenance a np:Provenance . dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_assertion { miriam-gene:672 a ncit:C16612 . lld:C0029925 a ncit:C7057 . dgn-gda:DGN3d0f372b4dd738ca9fcf7b2d759b5dbb sio:SIO_000628 miriam-gene:672, lld:C0029925; a sio:SIO_001121 . } dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_provenance { dgn-np:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_assertion dcterms:description "[Based on this study, it was very difficult to obtain precise data to prove the value of applying genetic testing of BRCA1 mutations in Taiwanese patients with sporadic epithelial ovarian cancers or sporadic PSPC and even with a family history of breast and/or ovarian cancer because of its rare event and because of the too small number of cases available in this study.]. 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:11059339; 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:NP299063.RAXUh1Ya-mkMgN1NN8PRGgQVD5v1l7i-jvmII9U0mfrqQ130_publicationInfo { this: dcterms:created "2016-05-13T12:44:01+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }