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Q58798982-0C916F29-F6E3-4CCB-9D61-36DBA8D0CCB1
Q58798982-0C916F29-F6E3-4CCB-9D61-36DBA8D0CCB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-0C916F29-F6E3-4CCB-9D61-36DBA8D0CCB1
A Loss-of-Function Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability
P932
Q58798982-0C916F29-F6E3-4CCB-9D61-36DBA8D0CCB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58798982-0C916F29-F6E3-4CCB-9D61-36DBA8D0CCB1
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
331ccf8f595979cf18253a226e4c9a7231899ea3
P932
6089338
http://www.w3.org/2001/XMLSchema#string