| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-99 |
Sentence |
denotes |
A method for the solubilization of a (1----3)-beta-D-glucan isolated from Saccharomyces cerevisiae. |
| T1 |
0-99 |
Sentence |
denotes |
A method for the solubilization of a (1----3)-beta-D-glucan isolated from Saccharomyces cerevisiae. |
| TextSentencer_T2 |
100-191 |
Sentence |
denotes |
This report describes a method for the solubilization of a micro-particulate beta-D-glucan. |
| T2 |
100-191 |
Sentence |
denotes |
This report describes a method for the solubilization of a micro-particulate beta-D-glucan. |
| TextSentencer_T3 |
192-300 |
Sentence |
denotes |
Insoluble glucan is dissolved in methyl sulfoxide and urea (8M) and partially phosphorylated at 100 degrees. |
| T3 |
192-300 |
Sentence |
denotes |
Insoluble glucan is dissolved in methyl sulfoxide and urea (8M) and partially phosphorylated at 100 degrees. |
| TextSentencer_T4 |
301-364 |
Sentence |
denotes |
The resulting water-soluble product is called glucan phosphate. |
| T4 |
301-364 |
Sentence |
denotes |
The resulting water-soluble product is called glucan phosphate. |
| TextSentencer_T5 |
365-477 |
Sentence |
denotes |
The conversion rate is 70%, and the preparation is endotoxin free as determined by the Limulus lysate procedure. |
| T5 |
365-477 |
Sentence |
denotes |
The conversion rate is 70%, and the preparation is endotoxin free as determined by the Limulus lysate procedure. |
| TextSentencer_T6 |
478-690 |
Sentence |
denotes |
Glucan phosphate is composed of 34.66% C, 6.29% H, 42.83% O, and 2.23% P and has a repeating-unit empirical formula of (C6H10O5)7.PO3H2, indicating a phosphate group substitution on every seventh glucose subunit. |
| T6 |
478-690 |
Sentence |
denotes |
Glucan phosphate is composed of 34.66% C, 6.29% H, 42.83% O, and 2.23% P and has a repeating-unit empirical formula of (C6H10O5)7.PO3H2, indicating a phosphate group substitution on every seventh glucose subunit. |
| TextSentencer_T7 |
691-949 |
Sentence |
denotes |
Molecular-weight averages, polydispersity, and intrinsic viscosity were determined by aqueous high-performance size-exclusion chromatography (s.e.c.) with on-line, multi-angle laser light scattering (m.a.l.l.s.) photometry and differential viscometry (d.v.). |
| T7 |
691-949 |
Sentence |
denotes |
Molecular-weight averages, polydispersity, and intrinsic viscosity were determined by aqueous high-performance size-exclusion chromatography (s.e.c.) with on-line, multi-angle laser light scattering (m.a.l.l.s.) photometry and differential viscometry (d.v.). |
| TextSentencer_T8 |
950-982 |
Sentence |
denotes |
Two polymer peaks were resolved. |
| T8 |
950-982 |
Sentence |
denotes |
Two polymer peaks were resolved. |
| TextSentencer_T9 |
983-1151 |
Sentence |
denotes |
Peak 1 (Mw = 3.57 x 10(6) daltons), represents approximately 2% of the total polymers, while peak 2 (Mw = 1.10 x 10(5) daltons) comprises approximately 98% of polymers. |
| T9 |
983-1151 |
Sentence |
denotes |
Peak 1 (Mw = 3.57 x 10(6) daltons), represents approximately 2% of the total polymers, while peak 2 (Mw = 1.10 x 10(5) daltons) comprises approximately 98% of polymers. |
| TextSentencer_T10 |
1152-1265 |
Sentence |
denotes |
13C- and 31P-n.m.r. spectroscopy confirmed the beta-1,3 interchain linkage and the presence of a phosphate group. |
| T10 |
1152-1265 |
Sentence |
denotes |
13C- and 31P-n.m.r. spectroscopy confirmed the beta-1,3 interchain linkage and the presence of a phosphate group. |
| TextSentencer_T11 |
1266-1352 |
Sentence |
denotes |
In solution, glucan phosphate polymers self-associate in a triple-helical arrangement. |
| T11 |
1266-1352 |
Sentence |
denotes |
In solution, glucan phosphate polymers self-associate in a triple-helical arrangement. |
| TextSentencer_T12 |
1353-1522 |
Sentence |
denotes |
The ability to prepare a immunologically active, non-toxic, water-soluble beta-D-glucan preparation will greatly enhance the clinical utility of this class of compounds. |
| T12 |
1353-1522 |
Sentence |
denotes |
The ability to prepare a immunologically active, non-toxic, water-soluble beta-D-glucan preparation will greatly enhance the clinical utility of this class of compounds. |