@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:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_head { this: np:hasAssertion dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_assertion; np:hasProvenance dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_provenance; np:hasPublicationInfo dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_publicationInfo; a np:Nanopublication . dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_assertion a np:Assertion . dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_provenance a np:Provenance . dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_publicationInfo a np:PublicationInfo . } dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_assertion { miriam-gene:208 a ncit:C16612 . lld:C1140680 a ncit:C7057 . dgn-gda:DGN9d1f5fe888888e7c54e8913de2dcc0ec sio:SIO_000628 miriam-gene:208, lld:C1140680; a sio:SIO_001121 . } dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_provenance { dgn-np:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_assertion dcterms:description "[Despite the relatively high prevalence of ovarian cancer (1% of American women will develop this disease in their lifetime) and recent developments in its molecular genetic understanding (several proto-oncogenes, such as AKT2 and cKRAS, and tumor suppressor genes, such as BRCA1 and BRCA2, have been implicated), little is known about the presence of ovarian tumors and cancer in women already diagnosed with other familial multiple tumor syndromes.]. 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:12144681; 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:NP362785.RAiRfHAzj9FfQjglcbwryw2cwr41IYAq4358DUm8iEKz8130_publicationInfo { this: dcterms:created "2016-05-13T12:44:30+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" . }