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Q52237907-C9BEAF00-70F9-4237-83CF-5FB234EFA330
Q52237907-C9BEAF00-70F9-4237-83CF-5FB234EFA330
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52237907-C9BEAF00-70F9-4237-83CF-5FB234EFA330
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita.
P50
Q52237907-C9BEAF00-70F9-4237-83CF-5FB234EFA330
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52237907-C9BEAF00-70F9-4237-83CF-5FB234EFA330
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
fd317a4abb8072830a1d5cecb1c8435a43408265
P1545
1
http://www.w3.org/2001/XMLSchema#string
P50
M Stuhrmann