@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:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_head { this: np:hasAssertion dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_assertion; np:hasProvenance dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_provenance; np:hasPublicationInfo dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_publicationInfo; a np:Nanopublication . dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_assertion a np:Assertion . dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_provenance a np:Provenance . dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_publicationInfo a np:PublicationInfo . } dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_assertion { miriam-gene:10587 a ncit:C16612 . lld:C1846502 a ncit:C7057 . dgn-gda:DGN7809f7bb8dd37d0970218c3057e053e9 sio:SIO_000628 miriam-gene:10587, lld:C1846502; a sio:SIO_001122 . } dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_provenance { dgn-np:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_assertion dcterms:description "[Two variants, 6q25.1-rs9383938 and TXNRD2-rs8141691, were statistically significantly associated with percent MD (P = 0.019 and 0.03, respectively), with the 6q25.1-rs9383938 association being consistent with the SNP effect on breast 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:25002657; 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:NP1199362.RA2s8h_yNLLMmOtvHFKB7sXJKB8DVDz-BFpNAc0EsuCdE130_publicationInfo { this: dcterms:created "2016-05-13T12:50:49+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" . }