PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12522561-1	2003	Mucopolysaccharidosis VII (MPS VII) is an autosomal recessive disorder caused by the deficiency of beta-glucuronidase leading to the intralysosomal storage of heparan, dermatan, and chondroitin sulfate.	Dermatan Sulfate	168-176	glucuronidase beta	Homo sapiens	99-117	
6423280-0	1983	Selective depolymerisation of dermatan sulfate: production of radiolabelled substrates for alpha-L-iduronidase, sulfoiduronate sulfatase, and beta-D-glucuronidase.	Dermatan Sulfate	30-46	glucuronidase beta	Homo sapiens	142-162	
6423280-1	1983	Radiolabelled disaccharide substrates for alpha-L-iduronidase, beta-D-glucuronidase, and sulfoiduronate sulfatase have been prepared from dermatan sulfate by application in sequence of N-deacetylation, deaminative cleavage, and reduction with NaBT4.	Dermatan Sulfate	138-154	glucuronidase beta	Homo sapiens	63-113	
9268591-7	1997	A significant decrease of dermatan sulfate levels with aging correlates well with the observed increase in the level of beta-glucuronidase activity.	Dermatan Sulfate	26-42	glucuronidase beta	Homo sapiens	120-138