PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33213094-2	2020	The primary mechanism of organophosphorus toxicity is through inhibition of the enzyme acetylcholinesterase, with current emergency treatment including anticholinergics, benzodiazepines, and oxime reactivators.	Oximes	191-196	acetylcholinesterase	Danio rerio	87-107	
33213094-7	2020	Additionally, the organophosphorus-specific response for oxime reactivation of acetylcholinesterase was comparable to what has been previously reported.	Oximes	57-62	acetylcholinesterase	Danio rerio	79-99	
25701203-2	2015	Here we evaluated the zebrafish as a potential pharmacological model for screening novel oxime antidotes to organophosphate (OP)-inhibited acetylcholinesterase (AChE).	Oximes	89-94	acetylcholinesterase	Danio rerio	161-165	
25701203-5	2015	However, differences between the Kox and k2 constants suggest that zebrafish AChE associates more tightly with oximes, but has a slower maximal reactivation rate than human AChE.	Oximes	111-117	acetylcholinesterase	Danio rerio	77-81