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Q64885040-4B84CF1C-9268-4217-A85B-CF8DE9EA6368
Q64885040-4B84CF1C-9268-4217-A85B-CF8DE9EA6368
BestRank
Statement
http://www.wikidata.org/entity/statement/Q64885040-4B84CF1C-9268-4217-A85B-CF8DE9EA6368
Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
P2093
Q64885040-4B84CF1C-9268-4217-A85B-CF8DE9EA6368
BestRank
Statement
http://www.wikidata.org/entity/statement/Q64885040-4B84CF1C-9268-4217-A85B-CF8DE9EA6368
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
8277c002222c46ec603737590a6a1c469d398d21
P1545
10
http://www.w3.org/2001/XMLSchema#string
P2093
Shigeru Nomura
http://www.w3.org/2001/XMLSchema#string