@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:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_head { this: np:hasAssertion dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_assertion; np:hasProvenance dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_provenance; np:hasPublicationInfo dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_publicationInfo; a np:Nanopublication . dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_assertion a np:Assertion . dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_provenance a np:Provenance . dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_publicationInfo a np:PublicationInfo . } dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_assertion { miriam-gene:1956 a ncit:C16612 . lld:C0152013 a ncit:C7057 . dgn-gda:DGNa3b9395c1c6a976c35a387cf5d732f91 sio:SIO_000628 miriam-gene:1956, lld:C0152013; a sio:SIO_001121 . } dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_provenance { dgn-np:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_assertion dcterms:description "[c-MYC gain (but not chromosome 8 gain or c-MYC amplification) was an independent poor-prognostic factor in the full cohort of lung adenocarcinoma (P=0.022, hazard ratio (HR)=1.71, 95% confidence interval (CI), 1.08-2.69 for DFS; P=0.032, HR=2.04, 95% CI, 1.06-3.91 for OS), as well as in stage I subgroup (P=0.023, HR=4.70, 95% CI, 1.24-17.78 for DFS; P=0.031, HR=4.65, 95% CI, 1.15-18.81 for OS), and in EGFR-mutant subgroup (P=0.022; HR=2.14; 95% CI, 1.11-4.10 for DFS).]. 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:24809777; 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:NP1180576.RAxAa8a5MOCS1PMikMq_LtKVpol_JY7wptojV_N3mPzgA130_publicationInfo { this: dcterms:created "2016-05-13T12:50:41+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" . }