PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8879146-7	1996	5-OH-NEF formation was inhibited by antibody to rat CYP3A2 by 60%, and antibodies to CYP2B1, CYP2C11 and CYP2E1 also showed 15-25% inhibition of the formation of 5-OH-NEF.	5-oh	0-4	S100 calcium binding protein B	Homo sapiens	5-8	
8879146-7	1996	5-OH-NEF formation was inhibited by antibody to rat CYP3A2 by 60%, and antibodies to CYP2B1, CYP2C11 and CYP2E1 also showed 15-25% inhibition of the formation of 5-OH-NEF.	5-oh	0-4	cytochrome P450, family 3, subfamily a, polypeptide 2	Rattus norvegicus	52-58	
8879146-7	1996	5-OH-NEF formation was inhibited by antibody to rat CYP3A2 by 60%, and antibodies to CYP2B1, CYP2C11 and CYP2E1 also showed 15-25% inhibition of the formation of 5-OH-NEF.	5-oh	0-4	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	105-111	
8879146-7	1996	5-OH-NEF formation was inhibited by antibody to rat CYP3A2 by 60%, and antibodies to CYP2B1, CYP2C11 and CYP2E1 also showed 15-25% inhibition of the formation of 5-OH-NEF.	5-oh	0-4	S100 calcium binding protein B	Homo sapiens	167-170	
8879146-12	1996	NEF metabolism in microsomes prepared from B-lymphoblastoid cells expressing human cytochrome P450s showed that 5-OH-NEF formation by CYP3A4 is the principal metabolic pathway in humans.	5-oh	112-116	S100 calcium binding protein B	Homo sapiens	0-3	
8879146-12	1996	NEF metabolism in microsomes prepared from B-lymphoblastoid cells expressing human cytochrome P450s showed that 5-OH-NEF formation by CYP3A4 is the principal metabolic pathway in humans.	5-oh	112-116	S100 calcium binding protein B	Homo sapiens	117-120	
8879146-12	1996	NEF metabolism in microsomes prepared from B-lymphoblastoid cells expressing human cytochrome P450s showed that 5-OH-NEF formation by CYP3A4 is the principal metabolic pathway in humans.	5-oh	112-116	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	134-140