PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
25019929-1	2014	The stereoselective synthesis of (+)-antimycin A1b has been accomplished in 12 linear steps and 18% overall yield from (-)-ethyl lactate.	ethyl lactate	119-136	syntrophin beta 1	Homo sapiens	47-50
9341082-5	1997	For one of these series (Nusplingen, district Balingen, Schwabische A1b), habitat specific properties have already been assumed to be responsible for an insufficient iron supply of the inhabitants.	Iron	166-170	syntrophin beta 1	Homo sapiens	68-71
16192269-0	2005	Purification of ATP-binding cassette transporter A1 and associated binding proteins reveals the importance of beta1-syntrophin in cholesterol efflux.	Cholesterol	130-141	syntrophin beta 1	Homo sapiens	110-126
16192269-6	2005	Small interference RNA inhibition of beta1-syntrophin expression reduced cholesterol efflux from primary skin fibroblasts by 50% while decreasing efflux 30% in bone marrow-derived macrophages.	Cholesterol	73-84	syntrophin beta 1	Homo sapiens	37-53
18306293-3	2008	In the reactions with alicyclic ketones, a highly enantioselective formation of anti-2-(3-phthalimido-1-hydroxypropyl)cycloketones 1a-1b (>99% ee) was observed.	alicyclic ketones	22-39	syntrophin beta 1	Homo sapiens	132-136
18306293-3	2008	In the reactions with alicyclic ketones, a highly enantioselective formation of anti-2-(3-phthalimido-1-hydroxypropyl)cycloketones 1a-1b (>99% ee) was observed.	2-(3-phthalimido-1-hydroxypropyl)cycloketones	85-130	syntrophin beta 1	Homo sapiens	132-136
11707114-1	2001	The stereospecific total synthesis of (+/-)-thielocin A1beta has been achieved from the common intermediate ethyl 5-formyl-2,4-dihydroxy-3,6-dimethyl benzoate (8).	ethyl 5-formyl-2,4-dihydroxy-3,6-dimethyl benzoate	108-158	syntrophin beta 1	Homo sapiens	54-60
11707114-3	2001	The resulting condensate (31) was homologated by successive esterification with protected monomeric phenol 41 to provide, after careful removal of the protecting groups, the desired thielocin A1beta.	Phenol	100-106	syntrophin beta 1	Homo sapiens	192-198
2944882-8	1986	On the other hand, E-P forming activity was still retained by A1b + B complex.	Glu-Pro	19-22	syntrophin beta 1	Homo sapiens	62-65
7844151-0	1995	Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus.	Carbonic Acid	103-107	syntrophin beta 1	Homo sapiens	10-40
3442600-6	1987	The A1b activator was characterized by the amino-acid compositions of all tryptic peptides and of the entire protein; sequencing was performed of the regions 1-34 and 42-56.	Peptides	82-90	syntrophin beta 1	Homo sapiens	4-7
3442600-9	1987	The difference between A1a and A1b activator is due to the carbohydrate part.	Carbohydrates	59-71	syntrophin beta 1	Homo sapiens	31-34
3442600-10	1987	The total amount of 49% carbohydrate in A1a and 76.7% in A1b consists mainly of hexoses.	Carbohydrates	24-36	syntrophin beta 1	Homo sapiens	57-60
2944882-11	1986	E-P formed with A1b + B complex was ADP-sensitive (E1-P), and was not further decomposed, since the transition from E1-P to E2-P was blocked.	Glu-Pro	0-3	syntrophin beta 1	Homo sapiens	16-19
2944882-11	1986	E-P formed with A1b + B complex was ADP-sensitive (E1-P), and was not further decomposed, since the transition from E1-P to E2-P was blocked.	Adenosine Diphosphate	36-39	syntrophin beta 1	Homo sapiens	16-19
2944882-11	1986	E-P formed with A1b + B complex was ADP-sensitive (E1-P), and was not further decomposed, since the transition from E1-P to E2-P was blocked.	e1-p	51-55	syntrophin beta 1	Homo sapiens	16-19
2944882-11	1986	E-P formed with A1b + B complex was ADP-sensitive (E1-P), and was not further decomposed, since the transition from E1-P to E2-P was blocked.	N,N-diethyl-2-(1-pyridyl)ethylamine	124-128	syntrophin beta 1	Homo sapiens	16-19
6840091-2	1983	Direct evidence is given for the presence of glucose, mannose and galactose as the products of hydrolysis of hemoglobins A1a1, A1a2, A1b, A1c and A0.	Glucose	45-52	syntrophin beta 1	Homo sapiens	133-136
6840091-2	1983	Direct evidence is given for the presence of glucose, mannose and galactose as the products of hydrolysis of hemoglobins A1a1, A1a2, A1b, A1c and A0.	Mannose	54-61	syntrophin beta 1	Homo sapiens	133-136
6840091-2	1983	Direct evidence is given for the presence of glucose, mannose and galactose as the products of hydrolysis of hemoglobins A1a1, A1a2, A1b, A1c and A0.	Galactose	66-75	syntrophin beta 1	Homo sapiens	133-136
6249380-4	1980	Addition of inositol hexaphosphate to nitrosyl hemoglobins A0, A1c, A1b and A1a-2 developed a triplet hyperfine structure of the EPR spectra but the magnitude of the hyperfine was decreased in the order of hemoglobins A0, A1c, A1b and A1a-2.	Phytic Acid	12-34	syntrophin beta 1	Homo sapiens	68-71
6249380-4	1980	Addition of inositol hexaphosphate to nitrosyl hemoglobins A0, A1c, A1b and A1a-2 developed a triplet hyperfine structure of the EPR spectra but the magnitude of the hyperfine was decreased in the order of hemoglobins A0, A1c, A1b and A1a-2.	Phytic Acid	12-34	syntrophin beta 1	Homo sapiens	227-230
31154909-2	2020	Some of the claimed negative health outcomes associated with milk consumption, such as cardiovascular diseases and type 1 diabetes may be attributed to an opioid peptide, beta-casomorphin-7 (BCM-7), derived from A1 beta-casein.	bcm	191-194	syntrophin beta 1	Homo sapiens	212-219
32816751-9	2021	SNTB1 rs7839488 was correlated with both AL (beta=0.07, p=0.005) and CR (beta=0.02, p=0.006).	Aluminum	41-43	syntrophin beta 1	Homo sapiens	0-5
32816751-9	2021	SNTB1 rs7839488 was correlated with both AL (beta=0.07, p=0.005) and CR (beta=0.02, p=0.006).	Chromium	69-71	syntrophin beta 1	Homo sapiens	0-5