PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31704607-0	2020	C-12 vs C-3 substituted bile salts: An example of the effects of substituent position and orientation on the self-assembly of steroid surfactant isomers.	Bile Acids and Salts	24-34	complement C3	Homo sapiens	8-11	
7150258-2	1982	Cholic acid was the major component, and related "atypical" bile acids included its C-3 and C-7 oxidation products, its 3 beta-epimer and 2 beta- and 6 alpha-hydroxylation products.	Bile Acids and Salts	60-70	complement C3	Homo sapiens	84-87	
7150258-7	1982	Bile acids lacking a substituent at C-12 included chenodeoxycholic acid, its C-3 and C-7 oxidation products, its 3 beta-epimer and its 6 alpha-hydroxylation product (hyocholic acid).	Bile Acids and Salts	0-10	complement C3	Homo sapiens	77-80	
864325-19	1977	All bile acids in the monosulfate fraction were conjugated and carried the sulfate ester group at C-3.	Bile Acids and Salts	4-14	complement C3	Homo sapiens	98-101	
32986170-7	2021	Complement component 3 (C3) was selected because of its regulation by bile acids and the glucoregulatory function of its proteolytically processed product C3adesArg or acylation-stimulating protein (ASP).	Bile Acids and Salts	70-80	complement C3	Homo sapiens	0-22	
25840355-11	2015	For the bile salt micelles to have GE (formation of secondary micelles) it is necessary that steroidal skeleton possesses C3-alpha-(e)-OH and C12-alpha-(a)-OH groups.	Bile Acids and Salts	8-17	complement C3	Homo sapiens	122-130	
22387310-0	2012	Structural requirements of bile acid transporters: C-3 and C-7 modifications of steroidal hydroxyl groups.	Bile Acids and Salts	27-36	complement C3	Homo sapiens	51-54	
22387310-2	2012	The objective of this study was to evaluate the effect of C-3 and C-7 substitution on bile acid interaction with these bile acid transporters.	Bile Acids and Salts	86-95	complement C3	Homo sapiens	58-61	
9990726-14	1998	Known bacterial biotranformations of conjugated bile acids include: deconjugation, oxidation of hydroxy groups at C-3, C-7 and C-12 with formation of oxo bile acids and reduction of these oxo groups to either alpha- or beta-configuration.	Bile Acids and Salts	48-58	complement C3	Homo sapiens	114-122	
1600374-1	1992	This paper describes a method for the direct gas/liquid chromatographic (GC) analysis of 46 glycine-conjugated bile acids, which differ from one another in the number, position and configuration of the hydroxyl groups at positions C-2, C-3, C-4, C-6, C-7 and/or C-12.	Bile Acids and Salts	111-121	complement C3	Homo sapiens	236-239	
1940629-4	1991	Improved methods are also described for the preparation of epimers of naturally occurring bile acids at C-3, C-7, and C-12.	Bile Acids and Salts	90-100	complement C3	Homo sapiens	104-107	
7806974-5	1994	Glucose conjugation was shown to occur at C-3 in all bile acid glucosides studied.	Bile Acids and Salts	53-62	complement C3	Homo sapiens	42-45	
1939467-3	1991	The separation of unconjugated and glycine- and taurine-conjugated bile acids with a C-3 oxo group has been carried out by high-performance liquid chromatography on a reversed-phase column.	Bile Acids and Salts	67-77	complement C3	Homo sapiens	85-88