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Q24675962-252DAAC3-4918-4B9B-A09E-E9B75CE33CB1
Q24675962-252DAAC3-4918-4B9B-A09E-E9B75CE33CB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24675962-252DAAC3-4918-4B9B-A09E-E9B75CE33CB1
Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1
P2860
Q24675962-252DAAC3-4918-4B9B-A09E-E9B75CE33CB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24675962-252DAAC3-4918-4B9B-A09E-E9B75CE33CB1
rank
NormalRank
type
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Statement
wasDerivedFrom
c4fff8312cf3b3f0926c5c1c2e5f6e517e32a741
P2860
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.