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Q44682405-8D2A14F2-5246-4AF9-BE97-59BC63ABD682
Q44682405-8D2A14F2-5246-4AF9-BE97-59BC63ABD682
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44682405-8D2A14F2-5246-4AF9-BE97-59BC63ABD682
Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutation.
P50
Q44682405-8D2A14F2-5246-4AF9-BE97-59BC63ABD682
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44682405-8D2A14F2-5246-4AF9-BE97-59BC63ABD682
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
5f2a656a02b56bcf517975fea22d2729a5cdf355
P1545
3
http://www.w3.org/2001/XMLSchema#string
P50
Julien Barbier