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Q47145435-7D272256-07E9-46EA-89E1-E4D084F444B3
Q47145435-7D272256-07E9-46EA-89E1-E4D084F444B3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-7D272256-07E9-46EA-89E1-E4D084F444B3
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.
P932
Q47145435-7D272256-07E9-46EA-89E1-E4D084F444B3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-7D272256-07E9-46EA-89E1-E4D084F444B3
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
823cb97ef770e75e83f475afdb3ef8b61fdad6a1
P932
5735936
http://www.w3.org/2001/XMLSchema#string