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Q37690192-D8F604D9-196A-484F-9F45-759AA32A8DB8
Q37690192-D8F604D9-196A-484F-9F45-759AA32A8DB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37690192-D8F604D9-196A-484F-9F45-759AA32A8DB8
Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype.
P2860
Q37690192-D8F604D9-196A-484F-9F45-759AA32A8DB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37690192-D8F604D9-196A-484F-9F45-759AA32A8DB8
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
18d35c214b0a34403f6841c0f5cfbc536c9e5390
P2860
WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.