Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_assertion type Assertion NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_head.
- NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_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." NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_provenance.
- NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_assertion evidence source_evidence_literature NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_provenance.
- NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_assertion SIO_000772 14729820 NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_provenance.
- NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_assertion wasDerivedFrom befree-20150227 NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_provenance.
- NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_assertion wasGeneratedBy ECO_0000203 NP586658.RAfQX0bEn0Bl7_kpx6zx3hxBaQe69FyVr5_dvF3h9sUYI130_provenance.