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
Q34340905-DABE40A6-1DAF-421B-8AFA-A80D00226756
Q34340905-DABE40A6-1DAF-421B-8AFA-A80D00226756
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34340905-DABE40A6-1DAF-421B-8AFA-A80D00226756
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.
P2860
Q34340905-DABE40A6-1DAF-421B-8AFA-A80D00226756
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34340905-DABE40A6-1DAF-421B-8AFA-A80D00226756
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
f4d44d7fb12e136ff3684ebf394bad3a5eb495ff
P2860
Autosomal recessive cerebellar ataxias: the current state of affairs.