PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19404589-2	2009	In this study, we demonstrated the constitutive immunoexpression of inducible nitric oxide synthase (iNOS) in the testis and epididymis of Wistar rats treated with finasteride for 28 days (the duration of two cycles of the seminiferous epithelium) and 56 days (the duration of one spermatogenesis).	Finasteride	164-175	nitric oxide synthase 2	Rattus norvegicus	68-99	
25864816-8	2015	RESULTS: Our data revealed that azelaic acid and finasteride significantly increased the expression of iNOS protein and nitric oxide (NO) levels in graft tissue (P < 0.05).	Finasteride	49-60	nitric oxide synthase 2	Rattus norvegicus	103-107	
19404589-2	2009	In this study, we demonstrated the constitutive immunoexpression of inducible nitric oxide synthase (iNOS) in the testis and epididymis of Wistar rats treated with finasteride for 28 days (the duration of two cycles of the seminiferous epithelium) and 56 days (the duration of one spermatogenesis).	Finasteride	164-175	nitric oxide synthase 2	Rattus norvegicus	101-105	
19404589-3	2009	We noted that a 56-day finasteride treatment mainly caused a decrease in the level of circulating DHT, as well as a statistically insignificant decrease in the level of T. The hormone deficiency also led to a change in the iNOS immnoexpression in the testis and epididymis of the finasteride-treated rats.	Finasteride	23-34	nitric oxide synthase 2	Rattus norvegicus	223-227	
19404589-3	2009	We noted that a 56-day finasteride treatment mainly caused a decrease in the level of circulating DHT, as well as a statistically insignificant decrease in the level of T. The hormone deficiency also led to a change in the iNOS immnoexpression in the testis and epididymis of the finasteride-treated rats.	Finasteride	280-291	nitric oxide synthase 2	Rattus norvegicus	223-227