PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23622383-11	2013	An increased concentration of NAA in the urine is sufficient to diagnose Canavan disease, which is due to mutations of the ASPA gene.	1-naphthaleneacetic acid	30-33	aspartoacylase	Homo sapiens	123-127	
26613958-1	2016	Canavan disease (CD) is a rare fatal childhood neurological autosomal recessive genetic disease caused by mutations in the ASPA gene, which lead to catalytic deficiency of the ASPA enzyme that catalyzes the deacetylation of NAA.	1-naphthaleneacetic acid	224-227	aspartoacylase	Homo sapiens	123-127	
26613958-1	2016	Canavan disease (CD) is a rare fatal childhood neurological autosomal recessive genetic disease caused by mutations in the ASPA gene, which lead to catalytic deficiency of the ASPA enzyme that catalyzes the deacetylation of NAA.	1-naphthaleneacetic acid	224-227	aspartoacylase	Homo sapiens	176-180	
1756590-1	1991	A new sensitive method for measuring aspartoacylase activity in human skin fibroblasts using [3H]N-acetyl-L-aspartic acid (NAA) is described.	1-naphthaleneacetic acid	123-126	aspartoacylase	Homo sapiens	37-51