@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:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_head { this: np:hasAssertion dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_assertion; np:hasProvenance dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_provenance; np:hasPublicationInfo dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_publicationInfo; a np:Nanopublication . dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_assertion a np:Assertion . dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_provenance a np:Provenance . dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_publicationInfo a np:PublicationInfo . } dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_assertion { miriam-gene:672 a ncit:C16612 . lld:C0006142 a ncit:C7057 . dgn-gda:DGN6197a55a53504a780126f28376257262 sio:SIO_000628 miriam-gene:672, lld:C0006142; a sio:SIO_001121 . } dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_provenance { dgn-np:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_assertion dcterms:description "[Given the large size of our study population and detailed analysis of the locus, this result indicates either that common variants in BRCA1 do not substantially influence sporadic breast cancer risk, or that unmeasured heterogeneity in the breast cancer phenotype or unmeasured interactions with genetic or environmental exposures obscure our ability to detect any influence that may be present.]. 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:16103107; 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:NP509056.RAogS34mZc2hfQM9Zq8Ou9ZpdnBRO_NPvjwhSpsAePlrU130_publicationInfo { this: dcterms:created "2016-05-13T12:45:35+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" . }