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
Q35578268-14AE4F6D-3CE7-4E7F-8BCF-F0B35393D253
Q35578268-14AE4F6D-3CE7-4E7F-8BCF-F0B35393D253
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35578268-14AE4F6D-3CE7-4E7F-8BCF-F0B35393D253
Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndrome
P2860
Q35578268-14AE4F6D-3CE7-4E7F-8BCF-F0B35393D253
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35578268-14AE4F6D-3CE7-4E7F-8BCF-F0B35393D253
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
1187c0d1a4da2215ba8a13d40f11026692b9e198
P2860
Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome.