Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_assertion description "[Here, we show that in human cancer, somatic mutations occur in the coding region of NRF2, especially among patients with a history of smoking or suffering from squamous cell carcinoma; in the latter case, this leads to poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_assertion evidence source_evidence_literature NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_assertion SIO_000772 18757741 NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_assertion wasDerivedFrom befree-20150227 NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_assertion wasGeneratedBy ECO_0000203 NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP589048.RAOD_hbJqeLt45PyrE6Gdhs82iuLy6WQ4OuGOuVDm9ypA130_provenance.