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1
Q51076518-42D7B32B-0882-4916-9DE8-B6FFC35549FD
Q51076518-42D7B32B-0882-4916-9DE8-B6FFC35549FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51076518-42D7B32B-0882-4916-9DE8-B6FFC35549FD
The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype.
P2093
Q51076518-42D7B32B-0882-4916-9DE8-B6FFC35549FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51076518-42D7B32B-0882-4916-9DE8-B6FFC35549FD
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
40556b4e179e211f79c5b39d622e23e94ca3af8a
P1545
3
http://www.w3.org/2001/XMLSchema#string
P2093
Arin Bhattacharjee
http://www.w3.org/2001/XMLSchema#string