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Q37132296-81DCA54B-30F6-4609-B353-3F0E2F373F77
Q37132296-81DCA54B-30F6-4609-B353-3F0E2F373F77
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132296-81DCA54B-30F6-4609-B353-3F0E2F373F77
Loss of NPC1 function in a patient with a co-inherited novel insulin receptor mutation does not grossly modify the severity of the associated insulin resistance.
P2860
Q37132296-81DCA54B-30F6-4609-B353-3F0E2F373F77
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132296-81DCA54B-30F6-4609-B353-3F0E2F373F77
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
11f0d1c9d698689588bd14065e03e3b978564e02
P2860
Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype