@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:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_head { this: np:hasAssertion dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_assertion; np:hasProvenance dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_provenance; np:hasPublicationInfo dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_publicationInfo; a np:Nanopublication . dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_assertion a np:Assertion . dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_provenance a np:Provenance . dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_publicationInfo a np:PublicationInfo . } dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_assertion { miriam-gene:675 a ncit:C16612 . lld:C0029925 a ncit:C7057 . dgn-gda:DGN9863c61e6a428ee9bad19c1ce5a4d81b sio:SIO_000628 miriam-gene:675, lld:C0029925; a sio:SIO_001121 . } dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_provenance { dgn-np:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_assertion dcterms:description "[Using multivariate analysis, the strongest predictors of detecting a mutation in BRCA1 or BRCA2 in this study group were the presence of a single family member with both breast and ovarian cancer (P <.0009; odds ratio [OR], 5.68; 95% confidence interval [CI], 2.04 to 15.76) and a young average age at breast cancer diagnosis in the family (P <.0016; OR, 1.69; 95% CI, 1.23 to 2.38).]. 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:11304778; 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:NP314587.RA_lDdTe2FgVP97pKQPyd5SVzhL98AAURA0gUzZ0prLA0130_publicationInfo { this: dcterms:created "2016-05-13T12:44:08+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" . }