PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10215790-0	1999	Sequence variations in the flavin-containing mono-oxygenase 3 gene (FMO3) in fish odour syndrome.	4,6-dinitro-o-cresol	27-33	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	68-72	
11266081-0	2001	A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria.	4,6-dinitro-o-cresol	24-30	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	62-66	
11266081-1	2001	Mutations of the flavin-containing monooxygenase type 3 gene (FMO3) that encode the major functional form present in adult human liver, have been shown to cause trimethylaminuria.	4,6-dinitro-o-cresol	17-23	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	62-66	
10215790-2	1999	Flavin-containing mono-oxygenase 3 (FMO3) catalyses TMA oxidation and mutations in the FMO3 gene have recently been shown to underlie trimethylaminuria/fish odour syndrome.	4,6-dinitro-o-cresol	0-6	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	36-40	
10215790-2	1999	Flavin-containing mono-oxygenase 3 (FMO3) catalyses TMA oxidation and mutations in the FMO3 gene have recently been shown to underlie trimethylaminuria/fish odour syndrome.	4,6-dinitro-o-cresol	0-6	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	87-91	
9398858-3	1997	TMA oxidation is catalyzed by flavin-containing mono-oxygenase (FMO; refs 7,8), and tissue localization and functional studies have established FMO3 as the form most likely to be defective in fish-odour syndrome.	4,6-dinitro-o-cresol	30-36	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	144-148	
34611047-6	2022	TMA then enters the liver through the portal vein circulation and is oxidised to trimethylamine oxide (TMAO) by the hepatic flavin-containing mono-oxygenase (FMO) family, especially FMO3.	4,6-dinitro-o-cresol	124-130	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	182-186	
26496755-4	2015	Moreover, sgRNA targeting flavin containing monooxygenases3 (Fmo3) gene and the corresponding single strand oligonucleotides (ssODN) donor template with point mutation were co-injected into the male pronucleus of one-cell mouse embryos stimulated HR-mediated repair mechanism.	4,6-dinitro-o-cresol	26-32	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	61-65	
9536088-0	1998	Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.	4,6-dinitro-o-cresol	17-23	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	55-59	
9536088-2	1998	We show here that mutations in the human flavin-containing monooxygenase isoform 3 gene ( FMO3 ) impair N -oxygenation of xenobiotics and are responsible for the trimethylaminuria phenotype.	4,6-dinitro-o-cresol	41-47	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	90-94	
9305407-1	1997	Variable amounts of flavin-containing monooxygenase isoforms 3 and 5 (FMO3 and FMO5) are present in microsomal preparations from adult, male, human liver.	4,6-dinitro-o-cresol	20-26	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	70-74