PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25228686-2	2014	Here, we have evaluated a potential role of WRN (mutated in Werner syndrome) and RECQ1 (the most abundant homolog of WRN) in hydroquinone (HQ)- and benzo[a]pyrene (BaP)-induced genotoxicity.	Benzo(a)pyrene	164-167	WRN RecQ like helicase	Homo sapiens	44-47	
25228686-3	2014	Silencing of WRN or RECQ1 expression in HeLa cells increased their sensitivity to HQ and BaP but elicited distinct DNA damage response.	Benzo(a)pyrene	89-92	WRN RecQ like helicase	Homo sapiens	13-16	
25228686-6	2014	Notably, loss of WRN in RECQ1-depleted cells ameliorated BaP toxicity.	Benzo(a)pyrene	57-60	WRN RecQ like helicase	Homo sapiens	17-20	
25228686-7	2014	Collectively, our results provide first indication of nonredundant participation of WRN and RECQ1 in protection from the potentially carcinogenic effects of BaP and HQ.	Benzo(a)pyrene	157-160	WRN RecQ like helicase	Homo sapiens	84-87	
16380375-3	2006	The results demonstrate that WRN helicase activity is inhibited in a strand-specific manner by BaP DE-dG adducts only when on the translocating strand.	Benzo(a)pyrene	95-98	WRN RecQ like helicase	Homo sapiens	29-32