| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-96 |
Sentence |
denotes |
Structure of an anti-complementary arabinogalactan from the root of Angelica acutiloba Kitagawa. |
| T1 |
0-96 |
Sentence |
denotes |
Structure of an anti-complementary arabinogalactan from the root of Angelica acutiloba Kitagawa. |
| TextSentencer_T2 |
97-338 |
Sentence |
denotes |
Mild acid hydrolysis of an anti-complementary arabinogalactan (AGIIb-1), isolated from the roots of Angelica acutiloba Kitagawa, gave one neutral (N-I) and two acidic arabinogalactan (A-I and A-II) units and one neutral arabinan unit (N-II). |
| T2 |
97-338 |
Sentence |
denotes |
Mild acid hydrolysis of an anti-complementary arabinogalactan (AGIIb-1), isolated from the roots of Angelica acutiloba Kitagawa, gave one neutral (N-I) and two acidic arabinogalactan (A-I and A-II) units and one neutral arabinan unit (N-II). |
| TextSentencer_T3 |
339-524 |
Sentence |
denotes |
The methyl-esterified rhamnogalacturonan cores of A-I and A-II were subjected to base-catalysed beta-elimination in the presence of sodium borodeuteride to give the neutral side-chains. |
| T3 |
339-524 |
Sentence |
denotes |
The methyl-esterified rhamnogalacturonan cores of A-I and A-II were subjected to base-catalysed beta-elimination in the presence of sodium borodeuteride to give the neutral side-chains. |
| TextSentencer_T4 |
525-757 |
Sentence |
denotes |
Gel filtration showed that A-I contained a high-molecular-weight arabinogalactan and two oligosaccharides consisting of Ara and Gal or Ara as the side chains, and that A-II was composed of two high-molecular-weight arabinogalactans. |
| T4 |
525-757 |
Sentence |
denotes |
Gel filtration showed that A-I contained a high-molecular-weight arabinogalactan and two oligosaccharides consisting of Ara and Gal or Ara as the side chains, and that A-II was composed of two high-molecular-weight arabinogalactans. |
| TextSentencer_T5 |
758-889 |
Sentence |
denotes |
Similar treatment of the acidic fraction, obtained by partial acid hydrolysis of A-I, gave mono- to tetra-galactosylgalactitol-1-d. |
| T5 |
758-889 |
Sentence |
denotes |
Similar treatment of the acidic fraction, obtained by partial acid hydrolysis of A-I, gave mono- to tetra-galactosylgalactitol-1-d. |
| TextSentencer_T6 |
890-1041 |
Sentence |
denotes |
Partial acid hydrolysis showed that the rhamnogalacturonan core of A-I contained the sequences --4)-GalA-(1--2)-Rha-(1-- and --4)-GalA-(1--4)-Rha-(1--. |
| T6 |
890-1041 |
Sentence |
denotes |
Partial acid hydrolysis showed that the rhamnogalacturonan core of A-I contained the sequences --4)-GalA-(1--2)-Rha-(1-- and --4)-GalA-(1--4)-Rha-(1--. |
| TextSentencer_T7 |
1042-1203 |
Sentence |
denotes |
Digestion with exo-beta-D-galactosidase and Smith degradation indicated that N-I contained a (1--3)-linked galactan backbone with 6-inked galactosyl side-chains. |
| T7 |
1042-1203 |
Sentence |
denotes |
Digestion with exo-beta-D-galactosidase and Smith degradation indicated that N-I contained a (1--3)-linked galactan backbone with 6-inked galactosyl side-chains. |
| TextSentencer_T8 |
1204-1292 |
Sentence |
denotes |
The galactan components of A-I and A-II contained chains that were rich in 3-linked Gal. |
| T8 |
1204-1292 |
Sentence |
denotes |
The galactan components of A-I and A-II contained chains that were rich in 3-linked Gal. |
| TextSentencer_T9 |
1293-1425 |
Sentence |
denotes |
Fluorescent-labelling with 2-aminopyridine indicated that Ara was the reducing terminal in N-II, whereas it was Rha in A-I and A-II. |
| T9 |
1293-1425 |
Sentence |
denotes |
Fluorescent-labelling with 2-aminopyridine indicated that Ara was the reducing terminal in N-II, whereas it was Rha in A-I and A-II. |
| TextSentencer_T10 |
1426-1703 |
Sentence |
denotes |
The mild acid treatment of a different AGIIb-1 preparation gave an oligosaccharide fraction which consisted mainly of terminal and 3-linked Arap, 4- or 5-linked Ara, terminal, 4-linked, and 4,6-linked Gal, and terminal GlcA, and contained Gal and Rha as the reducing terminals. |
| T10 |
1426-1703 |
Sentence |
denotes |
The mild acid treatment of a different AGIIb-1 preparation gave an oligosaccharide fraction which consisted mainly of terminal and 3-linked Arap, 4- or 5-linked Ara, terminal, 4-linked, and 4,6-linked Gal, and terminal GlcA, and contained Gal and Rha as the reducing terminals. |