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Q33906048-B310A8F0-7EC1-4970-BAD8-559494D0C22F
Q33906048-B310A8F0-7EC1-4970-BAD8-559494D0C22F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-B310A8F0-7EC1-4970-BAD8-559494D0C22F
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.
P50
Q33906048-B310A8F0-7EC1-4970-BAD8-559494D0C22F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-B310A8F0-7EC1-4970-BAD8-559494D0C22F
rank
NormalRank
type
BestRank
Statement
P1545
11
http://www.w3.org/2001/XMLSchema#string
P1932
Karin Jurkat-Rott
http://www.w3.org/2001/XMLSchema#string
P50
Karin Jurkat-Rott