@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:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_head { this: np:hasAssertion dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_assertion; np:hasProvenance dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_provenance; np:hasPublicationInfo dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_publicationInfo; a np:Nanopublication . dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_assertion a np:Assertion . dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_provenance a np:Provenance . dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_publicationInfo a np:PublicationInfo . } dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_assertion { miriam-gene:7098 a ncit:C16612 . lld:C0007131 a ncit:C7057 . dgn-gda:DGNbdbfaabe0a4088e1a9dc04c0ee768464 sio:SIO_000628 miriam-gene:7098, lld:C0007131; a sio:SIO_001122 . } dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_provenance { dgn-np:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_assertion dcterms:description "[Among the 178 SNPs, 24 were significantly associated with NSCLC prognosis in different genetic models and four of them were remained in the final predictive model after multivariate stepwise Cox regression, including IL-5R rs11713419 (5'-untranslated region, 5'-UTR) (P = 0.001), IL23R rs6682925 (5'-flanking region, 5'-FR) (P = 0.017), TLR1 rs5743551 (5'-FR) (P = 0.02) and TLR3 rs3775291 (Leu412Phe) (P = 0.01).]. 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:21412764; 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:NP880256.RANA5r2_IoomSkUGK_sHM1Tm2O_2ZbUUT2yqrURhJJov0130_publicationInfo { this: dcterms:created "2016-05-13T12:48:23+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" . }