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Q64885040-54FF4398-E8E8-4AB2-8A82-48D92DD86591
Q64885040-54FF4398-E8E8-4AB2-8A82-48D92DD86591
BestRank
Statement
http://www.wikidata.org/entity/statement/Q64885040-54FF4398-E8E8-4AB2-8A82-48D92DD86591
Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
P698
Q64885040-54FF4398-E8E8-4AB2-8A82-48D92DD86591
BestRank
Statement
http://www.wikidata.org/entity/statement/Q64885040-54FF4398-E8E8-4AB2-8A82-48D92DD86591
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
8277c002222c46ec603737590a6a1c469d398d21
P698
31164164
http://www.w3.org/2001/XMLSchema#string