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- NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_assertion type Assertion NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_head.
- NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_assertion wasGeneratedBy ECO_0000203 NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_provenance.
- NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_assertion wasDerivedFrom befree-2016 NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_provenance.
- NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_assertion SIO_000772 19646463 NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_provenance.
- NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_assertion evidence source_evidence_literature NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_provenance.
- NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_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." NP754730.RAjxDVZl-Hz9b_GlPeT2ZN0sUJhHegf6c_p_D_Ai_GWno130_provenance.