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1
Q53212278-774B7284-08FD-40F7-83F5-E5D89A63C1E8
Q53212278-774B7284-08FD-40F7-83F5-E5D89A63C1E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53212278-774B7284-08FD-40F7-83F5-E5D89A63C1E8
De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability.
P2093
Q53212278-774B7284-08FD-40F7-83F5-E5D89A63C1E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53212278-774B7284-08FD-40F7-83F5-E5D89A63C1E8
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
41f289557c2d20e7415ff2a86ec6a68b382f5aa7
P1545
8
http://www.w3.org/2001/XMLSchema#string
P2093
Pradeep C Vasudevan
http://www.w3.org/2001/XMLSchema#string