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
Q57484322-141BBAEA-B743-495D-8F67-85A1341DB306
Q57484322-141BBAEA-B743-495D-8F67-85A1341DB306
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-141BBAEA-B743-495D-8F67-85A1341DB306
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P2860
Q57484322-141BBAEA-B743-495D-8F67-85A1341DB306
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-141BBAEA-B743-495D-8F67-85A1341DB306
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
cddc5db81dd1747d2d348fa8b14e619569132815
P2860
Glial and neuronal isoforms of Neurofascin have distinct roles in the assembly of nodes of Ranvier in the central nervous system.