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Q36433297-1B729506-838B-43D8-9B83-A49B46BB328D
Q36433297-1B729506-838B-43D8-9B83-A49B46BB328D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36433297-1B729506-838B-43D8-9B83-A49B46BB328D
Further Delineation of the Phenotype of Congenital Disorder of Glycosylation DPAGT1-CDG (CDG-Ij) Identified by Homozygosity Mapping.
P2860
Q36433297-1B729506-838B-43D8-9B83-A49B46BB328D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36433297-1B729506-838B-43D8-9B83-A49B46BB328D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2addffeafbf7faa6a07c4c79aa69b379e8df4d5c
P2860
Idiopathic lactic acidemia with developmental delay and type 1 muscle fiber atrophy: report of two patients.