PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
34337561-1	2021	Hereditary sensory neuropathy type 1 (HSN1) is caused by mutations in the SPTLC1 or SPTLC2 sub-units of the enzyme serine palmitoyltransferase, resulting in the production of toxic 1-deoxysphingolipid bases (DSBs).	dsbs	208-212	serine palmitoyltransferase long chain base subunit 1	Homo sapiens	38-42	
34337561-1	2021	Hereditary sensory neuropathy type 1 (HSN1) is caused by mutations in the SPTLC1 or SPTLC2 sub-units of the enzyme serine palmitoyltransferase, resulting in the production of toxic 1-deoxysphingolipid bases (DSBs).	dsbs	208-212	serine palmitoyltransferase long chain base subunit 1	Homo sapiens	74-80	
20097765-3	2010	Here we show that the HSAN1 mutations induce a shift in the substrate specificity of SPT, which leads to the formation of the two atypical deoxy-sphingoid bases (DSBs) 1-deoxy-sphinganine and 1-deoxymethyl-sphinganine.	dsbs	162-166	serine palmitoyltransferase long chain base subunit 1	Homo sapiens	22-27