awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q34151650-01669B41-3377-430D-BCAD-D3947671F585
Q34151650-01669B41-3377-430D-BCAD-D3947671F585
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34151650-01669B41-3377-430D-BCAD-D3947671F585
Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation [corrected].
P2860
Q34151650-01669B41-3377-430D-BCAD-D3947671F585
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34151650-01669B41-3377-430D-BCAD-D3947671F585
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a763cfc98c8f714c77a25e1f8c17c8b0d557eacb
P2860
Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics.