PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
3276319-8	1988	Thus the enantiomeric composition of a metabolically formed dihydrodiol is determined by (i) the stereoselective epoxidation at a formal double bond of a parent hydrocarbon by microsomal cytochrome P-450 isozymes and (ii) the enantioselective and regioselective hydration of the metabolically formed epoxide by microsomal epoxide hydrolase.	trans-1,2-dihydro-1,2-naphthalenediol	60-71	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	187-203	
27299-2	1978	The yield of the dihydrodiol was maximal at pH 6.5, was reduced nicotinmide adenine dinucleotide phosphate- and cytochrome P-450-dependent, and was increased 2- to 4-fold by pretreatment of the animals with phenobarbital; pretreatment with 3-methylcholanthrene did not alter the activity of rat hepatic microsomes.	trans-1,2-dihydro-1,2-naphthalenediol	17-28	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	112-128