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Q54963859-614FA707-3C5B-42E8-B464-E48E053F0B6C
Q54963859-614FA707-3C5B-42E8-B464-E48E053F0B6C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-614FA707-3C5B-42E8-B464-E48E053F0B6C
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P2093
Q54963859-614FA707-3C5B-42E8-B464-E48E053F0B6C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-614FA707-3C5B-42E8-B464-E48E053F0B6C
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7495a00e1aa5a62977cadfded19d5519baa3826e
P1545
12
http://www.w3.org/2001/XMLSchema#string
P2093
Mohammad El-Khateeb
http://www.w3.org/2001/XMLSchema#string