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Q34249436-A0E7010D-F021-44E2-BD6F-D10B2A01E6C3
Q34249436-A0E7010D-F021-44E2-BD6F-D10B2A01E6C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34249436-A0E7010D-F021-44E2-BD6F-D10B2A01E6C3
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
P2860
Q34249436-A0E7010D-F021-44E2-BD6F-D10B2A01E6C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34249436-A0E7010D-F021-44E2-BD6F-D10B2A01E6C3
rank
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type
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Statement
wasDerivedFrom
d7e440d87dda92b792eb3b2a63d01e97b23a9aa7
P2860
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy