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
Q34629238-2A85BF53-9CFB-4B7E-B189-DFCEC6574FE1
Q34629238-2A85BF53-9CFB-4B7E-B189-DFCEC6574FE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34629238-2A85BF53-9CFB-4B7E-B189-DFCEC6574FE1
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
P2860
Q34629238-2A85BF53-9CFB-4B7E-B189-DFCEC6574FE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34629238-2A85BF53-9CFB-4B7E-B189-DFCEC6574FE1
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
fc215fd01f5536cd0ddf8ed6a6b1809039f12633
P2860
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.