Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_assertion> ?p ?o ?g. }
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- NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_assertion type Assertion NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_head.
- NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_assertion description "[While mutations in the NDUFS3 gene thus result in Leigh syndrome, a dissimilar clinical phenotype is observed in mutations in the NDUFV2 and NDUFS2 genes, resulting in encephalomyopathy and cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_provenance.
- NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_assertion evidence source_evidence_literature NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_provenance.
- NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_assertion SIO_000772 14729820 NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_provenance.
- NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_assertion wasDerivedFrom befree-20140225 NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_provenance.
- NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_assertion wasGeneratedBy ECO_0000203 NP330926.RArL2lvwb3ZuzbUHauFKv9t2w3lEsPkmggTIS24fMBGAk130_provenance.