Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_assertion> ?p ?o ?g. }
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- NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_assertion type Assertion NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_head.
- NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_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." NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_provenance.
- NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_assertion evidence source_evidence_curated NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_provenance.
- NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_assertion SIO_000772 14729820 NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_provenance.
- NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_assertion wasDerivedFrom ctd_human-20130708 NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_provenance.
- NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_assertion wasGeneratedBy ECO_0000218 NP23928.RAIKxuQEOvjHR--Txi8pgUgm-h9sHwdfTw3U9sHFUlJ90130_provenance.