@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:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_head { this: np:hasAssertion dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_assertion; np:hasProvenance dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_provenance; np:hasPublicationInfo dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_publicationInfo; a np:Nanopublication . dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_assertion a np:Assertion . dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_provenance a np:Provenance . dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_publicationInfo a np:PublicationInfo . } dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_assertion { miriam-gene:81448 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGNf5db00629d10a4ff9cfd7285a337b0fd sio:SIO_000628 miriam-gene:81448, lld:C0242379; a sio:SIO_001121 . } dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_provenance { dgn-np:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_assertion dcterms:description "[Meta-analysis of 30 studies suggested that individuals carrying Gln/Gln genotype were more likely than the individuals with Lys/Lys or Lys/Gln + Lys/Lys genotypes (homozygous model, OR 1.18, 95 % confidence interval (CI) 1.07-1.31; recessive model, OR 1.17, 95 % CI 1.06-1.29) to develop lung cancer, without any substantial heterogeneity.]. 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:24845027; 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:NP950797.RAYARsZHCTjsJ9Z_CAeK9N09HGJCt44dmD5NQvBYvksiw130_publicationInfo { this: dcterms:created "2015-08-25T14:47:20+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" . }