@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:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_head { this: np:hasAssertion dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_assertion; np:hasProvenance dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_provenance; np:hasPublicationInfo dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_publicationInfo; a np:Nanopublication . dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_assertion a np:Assertion . dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_provenance a np:Provenance . dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_publicationInfo a np:PublicationInfo . } dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_assertion { miriam-gene:7015 a ncit:C16612 . lld:C0242379 a ncit:C7057 . dgn-gda:DGN170d6e468b3d2f132bf230f8bc36ef12 sio:SIO_000628 miriam-gene:7015, lld:C0242379; a sio:SIO_001121 . } dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_provenance { dgn-np:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_assertion dcterms:description "[These results indicate that (a) the HBEC model system is a powerful new approach to assess the contribution of individual and combinations of genetic alterations to lung cancer pathogenesis; (b) a combination of four genetic alterations, including human telomerase reverse transcriptase overexpression, bypass of p16/RB and p53 pathways, and mutant K-RAS(V12) or mutant EGFR, is still not sufficient for HBECs to completely transform to cancer; and (c) EGFR tyrosine kinase inhibitors inhibit the growth of preneoplastic HBEC cells, suggesting their potential for chemoprevention.]. 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:16489012; 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:NP536514.RAh6qPFev2mvji5XX_S5-D6N7OS2vXJ-LC0O3JoUmeHy0130_publicationInfo { this: dcterms:created "2016-05-13T12:45:47+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" . }