PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22397046-1	2012	Sjogren-Larsson syndrome is an autosomal recessive neurocutaneous disease caused by mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, a microsomal enzyme that catalyzes the oxidation of medium- and long-chain aliphatic aldehydes fatty acids.	aliphatic aldehydes fatty acids	223-254	aldehyde dehydrogenase 3 family member A2	Homo sapiens	101-108	
22397046-1	2012	Sjogren-Larsson syndrome is an autosomal recessive neurocutaneous disease caused by mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, a microsomal enzyme that catalyzes the oxidation of medium- and long-chain aliphatic aldehydes fatty acids.	aliphatic aldehydes fatty acids	223-254	aldehyde dehydrogenase 3 family member A2	Homo sapiens	118-146