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Q33906048-B41BB7CF-0FB6-4379-9CFB-E7EC260C104F
Q33906048-B41BB7CF-0FB6-4379-9CFB-E7EC260C104F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-B41BB7CF-0FB6-4379-9CFB-E7EC260C104F
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.
P577
Q33906048-B41BB7CF-0FB6-4379-9CFB-E7EC260C104F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-B41BB7CF-0FB6-4379-9CFB-E7EC260C104F
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d810c90d0fe9bc22012c57fc0927c096edcccb59
P577
2003-09-10T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P577
d674a33ae724e7f3bdd4f02709d7595a