Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_assertion> ?p ?o ?g. }
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- NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_assertion type Assertion NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_head.
- NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_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." NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_provenance.
- NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_assertion evidence source_evidence_literature NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_provenance.
- NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_assertion SIO_000772 14729820 NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_provenance.
- NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_assertion wasDerivedFrom befree-20150227 NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_provenance.
- NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_assertion wasGeneratedBy ECO_0000203 NP586758.RAklcIY7yryuMpPnvUOR5h9sG8Gc8UJNUK0gKWc0a1eGY130_provenance.