PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9856490-1	1998	Thiamine-responsive megaloblastic anemia (TRMA, also known as Rogers syndrome, OMIM 249270) is a rare autosomal recessive disorder characterized by a triad of megaloblastic anemia, diabetes mellitus, and sensorineural deafness.	Thiamine	0-8	solute carrier family 19 member 2	Homo sapiens	42-46	
9856490-7	1998	The multi-system manifestations of TRMA suggest that thiamine has a pivotal role in a multiplicity of physiological processes.	Thiamine	53-61	solute carrier family 19 member 2	Homo sapiens	35-39	
9856490-8	1998	Mapping the TRMA gene and understanding the molecular basis of the disease might, thus, shed light on the role of thiamine in common disorders such as deafness, anemia, and diabetes.	Thiamine	114-122	solute carrier family 19 member 2	Homo sapiens	12-16