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Q47145435-25D7041F-B574-4DE6-8AED-89870E38B937
Q47145435-25D7041F-B574-4DE6-8AED-89870E38B937
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-25D7041F-B574-4DE6-8AED-89870E38B937
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.
P1476
Q47145435-25D7041F-B574-4DE6-8AED-89870E38B937
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47145435-25D7041F-B574-4DE6-8AED-89870E38B937
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
823cb97ef770e75e83f475afdb3ef8b61fdad6a1
P1476
Common founder effects of here
......
ns in the WHRN and TMC1 genes.
@en