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1
bb97818062ef8d02882e5f7be7d1b869da4ce336
bb97818062ef8d02882e5f7be7d1b869da4ce336
Reference
http://www.wikidata.org/reference/bb97818062ef8d02882e5f7be7d1b869da4ce336
Q21119445-3A4B0F50-C7F0-4B9B-811B-77CA838EE171
Q21119445-C0B75E65-7C94-43D1-8F58-A262AB665F0C
wasDerivedFrom
bb97818062ef8d02882e5f7be7d1b869da4ce336
Reference
http://www.wikidata.org/reference/bb97818062ef8d02882e5f7be7d1b869da4ce336
type
Reference
P1640
UniProt
P248
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
UniProt-GOA
P352
Q10469
http://www.w3.org/2001/XMLSchema#string
P459
IMP
P813
2019-04-08T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P854
annotations?geneProductId=UniProtKB:Q10469
P352
Q10469
P813
b441aa14f32ad7a9e6fe04eb80002b4c