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
Q38702643-B8C41C95-0151-4D30-987A-943767513FD2
Q38702643-B8C41C95-0151-4D30-987A-943767513FD2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38702643-B8C41C95-0151-4D30-987A-943767513FD2
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
P2860
Q38702643-B8C41C95-0151-4D30-987A-943767513FD2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38702643-B8C41C95-0151-4D30-987A-943767513FD2
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
390f2d9e0cfc95599c2f3a3b94862df405206f2e
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.