wikimedia
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Triples
Insights
Schema
BETA
Class frequency
Class hierarchy
SPARQL
GraphQL
BETA
Graphs
1
Q35670536-AF55FB38-89BF-4A70-8283-9A0A11205043
Q35670536-AF55FB38-89BF-4A70-8283-9A0A11205043
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35670536-AF55FB38-89BF-4A70-8283-9A0A11205043
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.
P2860
Q35670536-AF55FB38-89BF-4A70-8283-9A0A11205043
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35670536-AF55FB38-89BF-4A70-8283-9A0A11205043
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
21d562781a87c24ec10928bd7dc67a7afa058bb6
P2860
Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations.