@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:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_head { this: np:hasAssertion dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_assertion; np:hasProvenance dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_provenance; np:hasPublicationInfo dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_publicationInfo; a np:Nanopublication . dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_assertion a np:Assertion . dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_provenance a np:Provenance . dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_publicationInfo a np:PublicationInfo . } dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_assertion { miriam-gene:328 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGN887681d7878d61297dff70d7850794ff sio:SIO_000628 miriam-gene:328, lld:C0242379; a sio:SIO_001122 . } dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_provenance { dgn-np:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_assertion dcterms:description "[This study examines the association between 24 single-nucleotide polymorphisms (SNPs) belonging to five BER genes (XRCC1, APEX1, PARP1, MUTYH and OGG1) and lung cancer among Latinos (113 cases and 299 controls) and African-Americans (255 cases and 280 controls).]. 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:19029194; 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:NP59151.RA25AXy3vT7HH4il1XaUPUJv0yX5yY0pljj2Js0pVkLLE130_publicationInfo { this: dcterms:created "2015-08-25T14:38:12+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" . }