PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26863430-0	2016	Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy.	Thiamine	64-72	solute carrier family 19 member 3	Homo sapiens	6-13	
26863430-1	2016	BACKGROUND: Biotin-thiamine responsive basal ganglia disease is a severe, but potentially treatable disorder caused by mutations in the SLC19A3 gene.	Thiamine	19-27	solute carrier family 19 member 3	Homo sapiens	136-143