@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:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_head { this: np:hasAssertion dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_assertion; np:hasProvenance dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_provenance; np:hasPublicationInfo dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_publicationInfo; a np:Nanopublication . dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_assertion a np:Assertion . dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_provenance a np:Provenance . dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_assertion { miriam-gene:1571 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGNc141ed5c9fc8069fa03109669850f438 sio:SIO_000628 miriam-gene:1571, lld:C0242379; a sio:SIO_001121 . } dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_provenance { dgn-np:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_assertion dcterms:description "[We therefore assessed the genotype frequencies of PstI or RsaI CYP2E1 restriction fragment length polymorphisms and another susceptibility marker, mutagen sensitivity, in 137 lung cancer cases (92 African American and 45 Mexican American) and 206 controls (114 African American and 92 Mexican American) identified in a molecular epidemiological study of lung cancer.]. 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:9163682; 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:NP1373559.RAIcA3Q2EkYUF_TjWXDFcG5njQmKUkGmbRa08JmIrfmIU130_publicationInfo { this: dcterms:created "2016-05-13T12:52:08+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" . }