PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15016149-0	2002	TRMA syndrome (thiamine-responsive megaloblastic anemia): a case report and review of the literature.	Thiamine	15-23	solute carrier family 19 member 2	Homo sapiens	0-4	
15016149-1	2002	Thiamine-responsive megaloblastic anemia syndrome (TRMA) is an autosomal recessive disorder with features that include megaloblastic anemia, mild thrombocytopenia and leukopenia, sensorineural deafness and diabetes mellitus.	Thiamine	0-8	solute carrier family 19 member 2	Homo sapiens	51-55