Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_assertion wasGeneratedBy ECO_0000203 NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_assertion wasDerivedFrom befree-20150227 NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_assertion SIO_000772 19646463 NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_assertion evidence source_evidence_literature NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.
- NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_assertion description "[Association of loss of function with promoter polymorphisms in NRF2 or somatic and epigenetic mutations in KEAP1 and NRF2 has been found in cohorts of patients with acute lung injury/acute respiratory distress syndrome or lung cancer, which further supports the role for NRF2 in these lung diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416590.RAnQXFWoPBoa69N7iL1qM-51mno1pztXPL_bm9C2-5sCA130_provenance.