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1
Q43779485-8C96BF4C-5DB7-4CF4-949C-62A24CBB7E3D
Q43779485-8C96BF4C-5DB7-4CF4-949C-62A24CBB7E3D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43779485-8C96BF4C-5DB7-4CF4-949C-62A24CBB7E3D
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
P478
Q43779485-8C96BF4C-5DB7-4CF4-949C-62A24CBB7E3D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43779485-8C96BF4C-5DB7-4CF4-949C-62A24CBB7E3D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
36329b6c828850b75b5f14b0333300f2d261ddbc
P478
31
http://www.w3.org/2001/XMLSchema#string