@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:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_head { this: np:hasAssertion dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_assertion; np:hasProvenance dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_provenance; np:hasPublicationInfo dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_publicationInfo; a np:Nanopublication . dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_assertion a np:Assertion . dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_provenance a np:Provenance . dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_publicationInfo a np:PublicationInfo . } dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_assertion { miriam-gene:675 a ncit:C16612 . lld:C0346153 a ncit:C7057 . dgn-gda:DGNc050dbbeef06d4f1e38a5c8af8568928 sio:SIO_000628 miriam-gene:675, lld:C0346153; a sio:SIO_001121 . } dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_provenance { dgn-np:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_assertion dcterms:description "[A polygenic model in which many individually weak genes combine multiplicately to cause a 50-fold range of risk in the population explains several puzzling aspects of familial breast cancer epidemiology, including the very high risk in some families and the failure to identify important new genes since the discovery of BRCA1 and BRCA2.]. 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:12124169; 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:NP361603.RAk760_BFbGMIfB1F3Es3_jWc8bHs0cVFbf7p9oQL15E8130_publicationInfo { this: dcterms:created "2016-05-13T12:44:29+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" . }