@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:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_head { this: np:hasAssertion dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_assertion; np:hasProvenance dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_provenance; np:hasPublicationInfo dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_publicationInfo; a np:Nanopublication . dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_assertion a np:Assertion . dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_provenance a np:Provenance . dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_publicationInfo a np:PublicationInfo . } dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_assertion { miriam-gene:140468 a ncit:C16612 . lld:C0006142 a ncit:C7057 . dgn-gda:DGN2b3c1bb57f7b909dc182e574a8080e7d sio:SIO_000628 miriam-gene:140468, lld:C0006142; a sio:SIO_001122 . } dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_provenance { dgn-np:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_assertion dcterms:description "[Confirmed BC risk SNPs rs17468277 (CASP8), rs1982073 (TGFB1), rs2981582 (FGFR2), rs13281615 (8q24), rs3817198 (LSP1), rs889312 (MAP3K1), rs3803662 (TOX3), rs13387042 (2q35), rs4973768 (SLC4A7), rs6504950 (COX11) and rs10941679 (5p12) were genotyped for 25 853 BC patients with the available follow-up; 62 other SNPs, which have been suggested as BC risk SNPs by a GWAS or as candidate SNPs from individual studies, were genotyped for replication purposes in subsets of these patients.]. 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:22532573; 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:NP972928.RAt25PX-Oh0WTQ6ctioqhhhCAVWTWmG8ygqEpWNNl1dU0130_publicationInfo { this: dcterms:created "2015-08-25T14:47:34+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" . }