PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
3747715-5	1986	In contrast, mature male kidney S-9 fractions from all three strains had a significantly greater potential to activate DMN than mature female and immature animals.	Dimethylnitrosamine	119-122	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	Mus musculus	32-35	
7030474-1	1981	Dimethylnitrosamine (DMN) was mutagenic in the Salmonella plate incorporation assay (Ames test) at a level of 10 mumol/plate (3.7 mM) in the presence of hamster liver S-9.	Dimethylnitrosamine	0-19	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	Mus musculus	167-170	
7030474-1	1981	Dimethylnitrosamine (DMN) was mutagenic in the Salmonella plate incorporation assay (Ames test) at a level of 10 mumol/plate (3.7 mM) in the presence of hamster liver S-9.	Dimethylnitrosamine	21-24	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	Mus musculus	167-170	
7030474-2	1981	Mutagenicity of DMN at this level was not observed when the S-9 was derived from mouse or rat liver, although the mouse liver and hamster liver S-9 had similar DMN demethylase activities.	Dimethylnitrosamine	16-19	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	Mus musculus	60-63	
7030474-9	1981	The presence of an inhibitor of DMN activation in rat and mouse microsomes may account for, or contribute to, the failure of liver S-9 preparations from these species to activate DMN to a mutagen under standard conditions of the Ames test.	Dimethylnitrosamine	32-35	proteasome (prosome, macropain) 26S subunit, non-ATPase, 11	Mus musculus	131-134