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Q37115848-9D4D9AAB-73CD-4661-A53B-38845FD08964
Q37115848-9D4D9AAB-73CD-4661-A53B-38845FD08964
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37115848-9D4D9AAB-73CD-4661-A53B-38845FD08964
SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein
P2860
Q37115848-9D4D9AAB-73CD-4661-A53B-38845FD08964
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37115848-9D4D9AAB-73CD-4661-A53B-38845FD08964
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ba663b6676cbcbf3a2ede0bf30ee7eb1677acfb2
P2860
Autosomal recessive cerebellar ataxias: the current state of affairs.