Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_assertion> ?p ?o ?g. }
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- NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_assertion type Assertion NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_head.
- NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_assertion description "[Mutations found in this gene (NADH dehydrogenase iron-sulphur protein 3), coding for the seventh and last subunit of complex I core, were shown to cause late onset Leigh syndrome, optic atrophy, and complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_provenance.
- NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_assertion evidence source_evidence_literature NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_provenance.
- NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_assertion SIO_000772 14729820 NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_provenance.
- NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_assertion wasDerivedFrom befree-20150227 NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_provenance.
- NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_assertion wasGeneratedBy ECO_0000203 NP812321.RAiTJwE69owAa2zYtEa736KSIdIKhIv5Cm6plhPHa3VxE130_provenance.