PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19440493-1	2009	BACKGROUND: Polycyclic aromatic hydrocarbons (PAHs) may increase breast cancer risk, and the association may be modified by inherited differences in deactivation of PAH intermediates by glutathione S-transferases (GSTs).	Polycyclic Aromatic Hydrocarbons	12-44	glutathione S-transferase alpha 1	Homo sapiens	214-218	
19440493-1	2009	BACKGROUND: Polycyclic aromatic hydrocarbons (PAHs) may increase breast cancer risk, and the association may be modified by inherited differences in deactivation of PAH intermediates by glutathione S-transferases (GSTs).	Polycyclic Aromatic Hydrocarbons	46-50	glutathione S-transferase alpha 1	Homo sapiens	214-218	
7888077-5	1994	Finally, the induction of human GSTs by drugs or nutritional constituents would justify an interest for developing chemointervention strategies in populations highly exposed to carcinogens like aflatoxin B1 and polycyclic aromatic hydrocarbons.	Polycyclic Aromatic Hydrocarbons	211-243	glutathione S-transferase alpha 1	Homo sapiens	32-36	
15274625-1	2004	The ultimate diol epoxide carcinogens derived from polycyclic aromatic hydrocarbons, such as benzo[a]pyrene (BP), are metabolized primarily by glutathione (GSH) conjugation reaction catalyzed by GSH transferases (GSTs).	Polycyclic Aromatic Hydrocarbons	51-83	glutathione S-transferase alpha 1	Homo sapiens	213-217	
30694518-1	2019	Glutathione-S transferases (GSTs) are xenobiotic-conjugation enzymes involved in the detoxification process of heterocyclic aromatic amines and polycyclic aromatic hydrocarbons, widely recognized risk factors of colorectal cancer (CRC) development.	Polycyclic Aromatic Hydrocarbons	144-176	glutathione S-transferase alpha 1	Homo sapiens	28-32