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Q57484322-D3487F36-E5B9-40BC-9EC9-99187B61E21E
Q57484322-D3487F36-E5B9-40BC-9EC9-99187B61E21E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-D3487F36-E5B9-40BC-9EC9-99187B61E21E
Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia
P478
Q57484322-D3487F36-E5B9-40BC-9EC9-99187B61E21E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57484322-D3487F36-E5B9-40BC-9EC9-99187B61E21E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4c30540ed9f848fc2c2839f1cee643c7476f1750
P478
27
http://www.w3.org/2001/XMLSchema#string