@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:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_head { this: np:hasAssertion dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_assertion; np:hasProvenance dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_provenance; np:hasPublicationInfo dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_publicationInfo; a np:Nanopublication . dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_assertion a np:Assertion . dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_provenance a np:Provenance . dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_publicationInfo a np:PublicationInfo . } dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGN69f0bd1e9f3403410be82d8c473357ec sio:SIO_000628 miriam-gene:7157, lld:C0242379; a sio:SIO_001122 . } dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_provenance { dgn-np:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_assertion dcterms:description "[Four of the variants were found to be weakly associated with lung cancer risk with borderline significance: these were XRCC3 T241M heterozygote odds ratio (OR), 0.89; 95% confidence interval (95% CI), 0.79-0.99 and homozygote OR, 0.84; 95% CI, 0.71-1.00 based on 3,467 cases and 5,021 controls from 8 studies, XPD K751Q (heterozygote OR, 0.99; 95% CI, 0.89-1.10 and homozygote OR, 1.19; 95% CI, 1.02-1.39) based on 6,463 cases and 6,603 controls from 9 studies, and TP53 R72P (heterozygote OR, 1.14; 95% CI, 1.00-1.29 and homozygote OR, 1.20; 95% CI, 1.02-1.42) based on 3,610 cases and 5,293 controls from 6 studies.]. 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:18990748; prov:wasDerivedFrom dgn-void:gad-20130706; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP58602.RArXkoykI2uQ5w5hiaCBFedlNAbJYGSPL2jexfMPIOnbE130_publicationInfo { this: dcterms:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }