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Q44885653-8BC2018F-85F3-44E3-B686-A8C936244620
Q44885653-8BC2018F-85F3-44E3-B686-A8C936244620
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44885653-8BC2018F-85F3-44E3-B686-A8C936244620
A novel deletion mutation in the arginine vasopressin receptor 2 gene and skewed X chromosome inactivation in a female patient with congenital nephrogenic diabetes insipidus.
P356
Q44885653-8BC2018F-85F3-44E3-B686-A8C936244620
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44885653-8BC2018F-85F3-44E3-B686-A8C936244620
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a48fcc00322041eaee2e3bb38fcff85de0020490
P356
10.1007/BF03346263
http://www.w3.org/2001/XMLSchema#string
P356
BF03346263