Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_assertion> ?p ?o ?g. }
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- NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_assertion type Assertion NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_head.
- NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_assertion description "[The ND1 subunit gene of the mitochondrial NADH-ubiquinone oxidoreductase (complex I) is a hot spot for mutations causing Leber hereditary optic neuropathy and several mutations causing the mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome (MELAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_provenance.
- NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_assertion evidence source_evidence_literature NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_provenance.
- NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_assertion SIO_000772 16849371 NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_provenance.
- NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_assertion wasDerivedFrom befree-20150227 NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_provenance.
- NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_assertion wasGeneratedBy ECO_0000203 NP585902.RAg6pJTJ-s5yQ_U9p5d8wTjn7btA2lllk048NnMcetZwI130_provenance.