Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_assertion> ?p ?o ?g. }
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- NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_assertion type Assertion NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_head.
- NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_assertion description "[The largest subunit, SDHA, is mutated in patients with Leigh syndrome and late-onset optic atrophy, but has not as yet been identified as a factor in hereditary cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_provenance.
- NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_assertion evidence source_evidence_literature NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_provenance.
- NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_assertion SIO_000772 16288654 NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_provenance.
- NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_assertion wasDerivedFrom befree-20150227 NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_provenance.
- NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_assertion wasGeneratedBy ECO_0000203 NP688657.RARSyAAUTBGTYiXFfKuGXDEXKeR7UWAkCUIhQwmTUM-w8130_provenance.