PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23034980-1	2013	Sjogren-Larsson syndrome is an inherited disorder of lipid metabolism caused by mutations in the ALDH3A2 gene that codes for fatty aldehyde dehydrogenase, which results in accumulation of fatty aldehydes and alcohols and is characterized by ichthyosis, intellectual disability, and spastic diplegia/quadriplegia.	fatty aldehyde	188-203	aldehyde dehydrogenase 3 family member A2	Homo sapiens	97-104	
23034980-1	2013	Sjogren-Larsson syndrome is an inherited disorder of lipid metabolism caused by mutations in the ALDH3A2 gene that codes for fatty aldehyde dehydrogenase, which results in accumulation of fatty aldehydes and alcohols and is characterized by ichthyosis, intellectual disability, and spastic diplegia/quadriplegia.	fatty aldehyde	188-203	aldehyde dehydrogenase 3 family member A2	Homo sapiens	125-153	
23034980-1	2013	Sjogren-Larsson syndrome is an inherited disorder of lipid metabolism caused by mutations in the ALDH3A2 gene that codes for fatty aldehyde dehydrogenase, which results in accumulation of fatty aldehydes and alcohols and is characterized by ichthyosis, intellectual disability, and spastic diplegia/quadriplegia.	Alcohols	208-216	aldehyde dehydrogenase 3 family member A2	Homo sapiens	97-104	
23034980-1	2013	Sjogren-Larsson syndrome is an inherited disorder of lipid metabolism caused by mutations in the ALDH3A2 gene that codes for fatty aldehyde dehydrogenase, which results in accumulation of fatty aldehydes and alcohols and is characterized by ichthyosis, intellectual disability, and spastic diplegia/quadriplegia.	Alcohols	208-216	aldehyde dehydrogenase 3 family member A2	Homo sapiens	125-153