@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:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_head { this: np:hasAssertion dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_assertion; np:hasProvenance dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_provenance; np:hasPublicationInfo dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_publicationInfo; a np:Nanopublication . dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_assertion a np:Assertion . dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_provenance a np:Provenance . dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_publicationInfo a np:PublicationInfo . } dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_assertion { miriam-gene:675 a ncit:C16612 . lld:C0029925 a ncit:C7057 . dgn-gda:DGN99c912692e8da8ca37cc354a4189e4ca sio:SIO_000628 miriam-gene:675, lld:C0029925; a sio:SIO_001121 . } dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_provenance { dgn-np:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_assertion dcterms:description "[To offer potentially life-saving interventions for at-risk family members, we propose that every woman newly diagnosed with ovarian cancer be offered genetic testing for BRCA1 and BRCA2 genes because mutations in these genes are the strongest known predictors of ovarian cancer risk.]. 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:20093589; 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:NP788750.RAOc0nuYQnAcJmZ4A5z5KVTnturKf4kUAO-eCwcJyTg34130_publicationInfo { this: dcterms:created "2016-05-13T12:47:42+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" . }