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Q36098636-91E71131-FE59-4D23-A2F4-6A401C21029A
Q36098636-91E71131-FE59-4D23-A2F4-6A401C21029A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36098636-91E71131-FE59-4D23-A2F4-6A401C21029A
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease.
P50
Q36098636-91E71131-FE59-4D23-A2F4-6A401C21029A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36098636-91E71131-FE59-4D23-A2F4-6A401C21029A
rank
NormalRank
type
BestRank
Statement
P1545
10
http://www.w3.org/2001/XMLSchema#string
P1932
Matthew Lebo
http://www.w3.org/2001/XMLSchema#string
P50
Matthew S Lebo