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1
Q37732141-038EB1D0-7F0D-43CB-9AF5-7CE6F30FA695
Q37732141-038EB1D0-7F0D-43CB-9AF5-7CE6F30FA695
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37732141-038EB1D0-7F0D-43CB-9AF5-7CE6F30FA695
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling.
P50
Q37732141-038EB1D0-7F0D-43CB-9AF5-7CE6F30FA695
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37732141-038EB1D0-7F0D-43CB-9AF5-7CE6F30FA695
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7fbecf815907536bf5c9758e3d7dd31186ba24e6
P1545
35
http://www.w3.org/2001/XMLSchema#string
P50
S Orcesi