Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion> ?p ?o ?g. }
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- NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion type Assertion NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_head.
- NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_provenance.
- NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion evidence source_evidence_literature NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_provenance.
- NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion SIO_000772 21266382 NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_provenance.
- NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion wasDerivedFrom befree-20150227 NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_provenance.
- NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion wasGeneratedBy ECO_0000203 NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_provenance.