PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19416848-2	2009	The primary cause is mutation in the NAGLU gene, resulting in deficiency of alpha-N-acetylglucosaminidase and lysosomal accumulation of heparan sulfate.	Heparitin Sulfate	136-151	N-acetyl-alpha-glucosaminidase	Homo sapiens	37-42