@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:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_head { this: np:hasAssertion dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_assertion; np:hasProvenance dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_provenance; np:hasPublicationInfo dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_publicationInfo; a np:Nanopublication . dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_assertion a np:Assertion . dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_provenance a np:Provenance . dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_publicationInfo a np:PublicationInfo . } dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_assertion { miriam-gene:7508 a ncit:C16612 . lld:C0006142 a ncit:C7057 . dgn-gda:DGN44dcdbaf4fea3151aa2b0a8cc879b48e sio:SIO_000628 miriam-gene:7508, lld:C0006142; a sio:SIO_001122 . } dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_provenance { dgn-np:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_assertion dcterms:description "[Using data/samples collected from the first 752 Caucasians and 141 African-Americans in an ongoing case-control study, we examined the association between breast cancer risk and 18 non-synonymous single-nucleotide polymorphisms (nsSNPs) in four DNA repair pathways-(i) base excision repair: ADPRT V762A, APE1 D148E, XRCC1 R194W/R280H/R399Q and POLD1 R119H; (ii) nucleotide excision repair: ERCC2 D312N/K751Q, ERCC4 R415Q, ERCC5 D1104H and XPC A499V/K939Q; (iii) mismatch repair: MLH1 I219V, MSH3 R940Q/T1036A and MSH6 G39E and (iv) double-strand break repair: NBS1 E185Q and XRCC3 T241M.]. 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:18701435; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP76244.RAGjp-HcamvbsddzNgFU6d_vSOIq0dnXxBKUJFrIdIPTI130_publicationInfo { this: dcterms:created "2015-08-25T14:38:21+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" . }