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Q38659790-C3714E27-B5C4-4864-A327-53B4AB47A1DF
Q38659790-C3714E27-B5C4-4864-A327-53B4AB47A1DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38659790-C3714E27-B5C4-4864-A327-53B4AB47A1DF
N-glycoprotein macroheterogeneity: biological implications and proteomic characterization.
P2860
Q38659790-C3714E27-B5C4-4864-A327-53B4AB47A1DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38659790-C3714E27-B5C4-4864-A327-53B4AB47A1DF
rank
NormalRank
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Statement
wasDerivedFrom
110a27cc55164ca9fde605a55b995e756f6bd719
P2860
A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.