wikimedia
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q49052576-9C25F064-E341-48A9-87E6-45B53CD6C3E5
Q49052576-9C25F064-E341-48A9-87E6-45B53CD6C3E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49052576-9C25F064-E341-48A9-87E6-45B53CD6C3E5
Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion.
P2860
Q49052576-9C25F064-E341-48A9-87E6-45B53CD6C3E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49052576-9C25F064-E341-48A9-87E6-45B53CD6C3E5
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
cdd14f4305d043fa51b8b42b2e04c27deaf96646
P2860
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.