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Q34386122-A2AFF97C-BBF2-49B5-B224-B375CCD075A0
Q34386122-A2AFF97C-BBF2-49B5-B224-B375CCD075A0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34386122-A2AFF97C-BBF2-49B5-B224-B375CCD075A0
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.
P2860
Q34386122-A2AFF97C-BBF2-49B5-B224-B375CCD075A0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34386122-A2AFF97C-BBF2-49B5-B224-B375CCD075A0
rank
NormalRank
type
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Statement
wasDerivedFrom
b0c5ac3378025f963687162dbca308922b00857e
P2860
A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).