PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
11380424-0	2001	A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome.	Thiamine	63-71	solute carrier family 19 member 2	Homo sapiens	24-31	
11380424-4	2001	These data confirm that the SLC19A2 gene is the high-affinity thiamine carrier and that this novel mutation is responsible for TRMA syndrome.	Thiamine	62-70	solute carrier family 19 member 2	Homo sapiens	28-35