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Q33906048-552DDDEB-31B5-4E57-8625-F82D57CA5971
Q33906048-552DDDEB-31B5-4E57-8625-F82D57CA5971
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-552DDDEB-31B5-4E57-8625-F82D57CA5971
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.
P5875
Q33906048-552DDDEB-31B5-4E57-8625-F82D57CA5971
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-552DDDEB-31B5-4E57-8625-F82D57CA5971
rank
NormalRank
type
BestRank
Statement
P5875
10570224
http://www.w3.org/2001/XMLSchema#string