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- NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_assertion type Assertion NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_head.
- NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_assertion wasGeneratedBy ECO_0000203 NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_provenance.
- NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_assertion wasDerivedFrom befree-20140225 NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_provenance.
- NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_assertion SIO_000772 19646463 NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_provenance.
- NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_assertion evidence source_evidence_literature NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_provenance.
- NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_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." NP779117.RAN0FNgobErUReD72DNPdds43o8usS7I_OxtQRfVZqnLw130_provenance.