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Q64885040-30B907B1-0188-4E82-8F02-5DA8949F5C86
Q64885040-30B907B1-0188-4E82-8F02-5DA8949F5C86
BestRank
Statement
http://www.wikidata.org/entity/statement/Q64885040-30B907B1-0188-4E82-8F02-5DA8949F5C86
Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
P932
Q64885040-30B907B1-0188-4E82-8F02-5DA8949F5C86
BestRank
Statement
http://www.wikidata.org/entity/statement/Q64885040-30B907B1-0188-4E82-8F02-5DA8949F5C86
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
8277c002222c46ec603737590a6a1c469d398d21
P932
6549368
http://www.w3.org/2001/XMLSchema#string