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Q57484322-4A9D7118-F309-4CF9-8BB1-8AE5693BD295
Q57484322-4A9D7118-F309-4CF9-8BB1-8AE5693BD295
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-4A9D7118-F309-4CF9-8BB1-8AE5693BD295
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P2860
Q57484322-4A9D7118-F309-4CF9-8BB1-8AE5693BD295
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-4A9D7118-F309-4CF9-8BB1-8AE5693BD295
rank
NormalRank
type
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Statement
wasDerivedFrom
cddc5db81dd1747d2d348fa8b14e619569132815
P2860
Neurofascins are required to establish axonal domains for saltatory conduction