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Q52137131-DEEF47D4-7F1F-46BD-AF0D-6C05C8F23965
Q52137131-DEEF47D4-7F1F-46BD-AF0D-6C05C8F23965
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52137131-DEEF47D4-7F1F-46BD-AF0D-6C05C8F23965
A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
P356
Q52137131-DEEF47D4-7F1F-46BD-AF0D-6C05C8F23965
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52137131-DEEF47D4-7F1F-46BD-AF0D-6C05C8F23965
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0abee08e8308e9e2a974d76ad36c61ebe5dfe9cb
P356
10.1002/AJMG.A.37721
http://www.w3.org/2001/XMLSchema#string
P356
AJMG.A.37721