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Q35195883-0E97CE4F-5B75-4119-AE34-3C85D81E6988
Q35195883-0E97CE4F-5B75-4119-AE34-3C85D81E6988
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35195883-0E97CE4F-5B75-4119-AE34-3C85D81E6988
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.
P2860
Q35195883-0E97CE4F-5B75-4119-AE34-3C85D81E6988
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35195883-0E97CE4F-5B75-4119-AE34-3C85D81E6988
rank
NormalRank
type
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wasDerivedFrom
cb2864f40df5bbb9da9a1f55c53906b619a411a3
P2860
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.