@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:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_head { this: np:hasAssertion dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_assertion; np:hasProvenance dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_provenance; np:hasPublicationInfo dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_publicationInfo; a np:Nanopublication . dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_assertion a np:Assertion . dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_provenance a np:Provenance . dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_publicationInfo a np:PublicationInfo . } dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_assertion { miriam-gene:83990 a ncit:C16612 . lld:C0029925 a ncit:C7057 . dgn-gda:DGN84ff0214ed949334bd853c37a636986f sio:SIO_000628 miriam-gene:83990, lld:C0029925; a sio:SIO_001121 . } dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_provenance { dgn-np:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_assertion dcterms:description "[Thirty-one percent of ovarian carcinomas had a deleterious germline (24%) and/or somatic (9%) mutation in one or more of the 13 homologous recombination genes: BRCA1, BRCA2, ATM, BARD1, BRIP1, CHEK1, CHEK2, FAM175A, MRE11A, NBN, PALB2, RAD51C, and RAD51D.]. 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:24240112; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP954145.RAsSCDMUdbis81dZQdeWCV33MHEA_ajCiqoEfZrQ8C5Xc130_publicationInfo { this: dcterms:created "2015-08-25T14:47:22+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }