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Q57484322-876E0DE6-1059-4C2B-802E-FE6C2855792F
Q57484322-876E0DE6-1059-4C2B-802E-FE6C2855792F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-876E0DE6-1059-4C2B-802E-FE6C2855792F
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P698
Q57484322-876E0DE6-1059-4C2B-802E-FE6C2855792F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-876E0DE6-1059-4C2B-802E-FE6C2855792F
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4c30540ed9f848fc2c2839f1cee643c7476f1750
P698
30124836
http://www.w3.org/2001/XMLSchema#string