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Q38378683-2BB5920F-D6A8-429B-A8CC-41DE3AB7CCBF
Q38378683-2BB5920F-D6A8-429B-A8CC-41DE3AB7CCBF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38378683-2BB5920F-D6A8-429B-A8CC-41DE3AB7CCBF
Generation and degradation of free asparagine-linked glycans.
P2860
Q38378683-2BB5920F-D6A8-429B-A8CC-41DE3AB7CCBF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38378683-2BB5920F-D6A8-429B-A8CC-41DE3AB7CCBF
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wasDerivedFrom
83b480481252c4684f6c1ec231457c66e69d77f4
P2860
A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.