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Q57484322-3FA2142C-97E5-44A2-8DFB-8CF47A56A331
Q57484322-3FA2142C-97E5-44A2-8DFB-8CF47A56A331
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-3FA2142C-97E5-44A2-8DFB-8CF47A56A331
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P433
Q57484322-3FA2142C-97E5-44A2-8DFB-8CF47A56A331
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-3FA2142C-97E5-44A2-8DFB-8CF47A56A331
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4c30540ed9f848fc2c2839f1cee643c7476f1750
P433
21
http://www.w3.org/2001/XMLSchema#string