PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19347672-1	2009	Thiamine responsive megaloblastic anemia syndrome (TRMA) is a clinical triad characterized by thiamine-responsive anemia, diabetes mellitus and sensorineural deafness.	Thiamine	0-8	solute carrier family 19 member 2	Homo sapiens	51-55	
19347672-1	2009	Thiamine responsive megaloblastic anemia syndrome (TRMA) is a clinical triad characterized by thiamine-responsive anemia, diabetes mellitus and sensorineural deafness.	Thiamine	94-102	solute carrier family 19 member 2	Homo sapiens	51-55	
19347672-2	2009	We report a 4-year-old girl with TRMA whose anemia improved following administration of thiamine and this case report sensitizes the early diagnosis and treatment with thiamine in children presenting with anemia, diabetes and deafness.	Thiamine	88-96	solute carrier family 19 member 2	Homo sapiens	33-37	
19347672-2	2009	We report a 4-year-old girl with TRMA whose anemia improved following administration of thiamine and this case report sensitizes the early diagnosis and treatment with thiamine in children presenting with anemia, diabetes and deafness.	Thiamine	168-176	solute carrier family 19 member 2	Homo sapiens	33-37