PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23879813-4	2013	Voglibose is a representative antidiabetic drug possessing inhibitory activity towards human alpha-glucosidase; it blocked the proper N-glycan modification of tyrosinase, resulting in a dramatic reduction of the tyrosinase protein level by altering its stability and subsequently decreasing melanin production.	n-glycan	134-142	tyrosinase	Homo sapiens	159-169	
17222224-0	2007	Influence of N-glycan processing disruption on tyrosinase and melanin synthesis in HM3KO melanoma cells.	n-glycan	13-21	tyrosinase	Homo sapiens	47-57	
21625599-10	2011	Results herein suggest that individual N-glycan location is critical for the stability, regional folding control and secretion of human tyrosinase and explains some tyrosinase gene missense mutations associated with oculocutaneous albinism type I.	n-glycan	39-47	tyrosinase	Homo sapiens	136-146	
21625599-10	2011	Results herein suggest that individual N-glycan location is critical for the stability, regional folding control and secretion of human tyrosinase and explains some tyrosinase gene missense mutations associated with oculocutaneous albinism type I.	n-glycan	39-47	tyrosinase	Homo sapiens	165-175	
17222224-3	2007	Previous studies showed that the disruption of early ER N-glycan processing by deoxynojirimycin (DNJ), an inhibitor of alpha-glucosidase, suppresses tyrosinase enzymatic activity and melanogenesis.	n-glycan	56-64	tyrosinase	Homo sapiens	149-159	
11412044-2	2001	The role of conserved N-glycan sites in sorting, stability, and activity of tyrosinase family proteins was investigated using two family members from two different species, mouse gp75/tyrosinase-related protein (TRP)-1/Tyrp1 and human tyrosinase.	n-glycan	22-30	tyrosinase	Homo sapiens	76-86	
11412044-4	2001	Our results show that selected conserved N-glycan sites on tyrosinase family members are crucial for stability in the secretory pathway and endocytic compartment and for enzymatic activity.	n-glycan	41-49	tyrosinase	Homo sapiens	59-69