PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15990133-10	2006	Because DMBA oxidation produces a highly mutagenic metabolite and is finally catalyzed by CYP1B1, a relatively low PCB126 dose might produce the biological character to potentially increase the risk of DMBA-induced mammary carcinoma.	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	8-12	cytochrome P450, family 1, subfamily b, polypeptide 1	Rattus norvegicus	90-96	
15990133-4	2006	We investigated the hepatic expression of CYP1 and AhR following oral administration of DMBA (100 mg/kg b.w.)	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	88-92	cytochrome P450, family 1, subfamily b, polypeptide 1	Rattus norvegicus	42-46	
15990133-10	2006	Because DMBA oxidation produces a highly mutagenic metabolite and is finally catalyzed by CYP1B1, a relatively low PCB126 dose might produce the biological character to potentially increase the risk of DMBA-induced mammary carcinoma.	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	202-206	cytochrome P450, family 1, subfamily b, polypeptide 1	Rattus norvegicus	90-96	
12704664-6	2003	DMBA-induced increase in expression of CYP1A1, CYP1A2 and CYP1B1 mRNA was similarly blunted in DHEA-treated animals.	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	0-4	cytochrome P450, family 1, subfamily b, polypeptide 1	Rattus norvegicus	58-64	
11097088-11	2000	While both AhR-regulated CYP1A1 and CYP1B1 mRNAs were induced in breast tissue within 6 h of DMBA gavage, only CYP1B1 mRNA remained elevated in tumors.	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	93-97	cytochrome P450, family 1, subfamily b, polypeptide 1	Rattus norvegicus	36-42	
1332854-10	1992	DMBA and BP metabolism by PMSG-treated rat ovarian microsomes and untreated testicular microsomes are each completely inhibited by anti-P450RAP but are not inhibited by anti-P450IA1.	6,11-dimethylbenzo(b)naphtho(2,3-d)thiophene	0-4	cytochrome P450, family 1, subfamily b, polypeptide 1	Rattus norvegicus	136-143