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Q24675799-F8364593-27CB-4A62-975C-A3BEC2311D39
Q24675799-F8364593-27CB-4A62-975C-A3BEC2311D39
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24675799-F8364593-27CB-4A62-975C-A3BEC2311D39
Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development
P921
Q24675799-F8364593-27CB-4A62-975C-A3BEC2311D39
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24675799-F8364593-27CB-4A62-975C-A3BEC2311D39
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
17da9be1f8890cd10616e848aec6b571eb80d078
P921
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase