PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18441444-2	2008	The syndrome is caused by homozygous or compound heterozygous mutations in genes KCNQ1 and KCNE1, which are responsible for encoding the delayed rectifier repolarizing current, I(Ks).	Potassium	179-181	potassium voltage-gated channel subfamily E regulatory subunit 1	Homo sapiens	91-96