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- NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_assertion type Assertion NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_head.
- NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_assertion description "[Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_provenance.
- NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_assertion evidence source_evidence_literature NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_provenance.
- NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_assertion SIO_000772 12928484 NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_provenance.
- NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_assertion wasDerivedFrom befree-20140225 NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_provenance.
- NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_assertion wasGeneratedBy ECO_0000203 NP581917.RA_0r1Uiq0ys24AN_Fy7fDUs0Q8bjG_mt_xD3nHe-qEgM130_provenance.