> top > projects > sentences > docs > PubMed:2611781 > annotations

PubMed:2611781 JSONTXT 38 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

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.