PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28665968-1	2017	SLC19A3 deficiency, also called thiamine metabolism dysfunction syndrome-2 (THMD2; OMIM 607483), is an autosomal recessive neurodegenerative disorder caused by mutations in SLC19A3, the gene encoding thiamine transporter 2.	Thiamine	32-40	solute carrier family 19 member 3	Homo sapiens	76-81	
28665968-4	2017	These findings may bear some features of thiamine-deficient mice generated by pyrithiamine injection and a thiamine-deficient diet, suggesting that the primary cause of THMD2 could be thiamine pyrophosphate (TPP) deficiency.	Thiamine	41-49	solute carrier family 19 member 3	Homo sapiens	169-174	
28665968-9	2017	These results showed that acute neurodegeneration caused by thiamine deficiency is preventable in most parts, and prompt high-dose thiamine administration is critical for the treatment of THMD2.	Thiamine	131-139	solute carrier family 19 member 3	Homo sapiens	188-193