awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Triples
Insights
Schema
BETA
Class frequency
Class hierarchy
SPARQL
Graphs
1
Q47229502-9836B81A-3237-4CDD-B4E1-B672CC5BA34F
Q47229502-9836B81A-3237-4CDD-B4E1-B672CC5BA34F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47229502-9836B81A-3237-4CDD-B4E1-B672CC5BA34F
Regulatory variants of FOXG1 in the context of its topological domain organisation.
P2860
Q47229502-9836B81A-3237-4CDD-B4E1-B672CC5BA34F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47229502-9836B81A-3237-4CDD-B4E1-B672CC5BA34F
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
fc782af428d3a5285925e45b9b2d9ec720da0be4
P2860
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.