PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
21344635-1	2011	Niemann-Pick disease type C (NPC) is a rare autosomal recessive lysosomal storage disorder characterized by defective intracellular lipid trafficking, with secondary accumulation of free cholesterol, sphingosine, and glycosphingolipids.	Sphingosine	200-211	NPC intracellular cholesterol transporter 1	Homo sapiens	0-27	
21344635-1	2011	Niemann-Pick disease type C (NPC) is a rare autosomal recessive lysosomal storage disorder characterized by defective intracellular lipid trafficking, with secondary accumulation of free cholesterol, sphingosine, and glycosphingolipids.	Sphingosine	200-211	NPC intracellular cholesterol transporter 1	Homo sapiens	29-32