| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-128 |
Sentence |
denotes |
An improved method for the structural profiling of keratan sulfates: analysis of keratan sulfates from brain and ovarian tumors. |
| T1 |
0-128 |
Sentence |
denotes |
An improved method for the structural profiling of keratan sulfates: analysis of keratan sulfates from brain and ovarian tumors. |
| T1 |
0-128 |
Sentence |
denotes |
An improved method for the structural profiling of keratan sulfates: analysis of keratan sulfates from brain and ovarian tumors. |
| TextSentencer_T2 |
129-388 |
Sentence |
denotes |
A previously developed method for the structural fingerprinting of keratan sulfates (Brown et al., Glycobiology, 5, 311-317, 1995) has been adapted for use with oligosaccharides fluorescently labeled with 2-aminobenzoic acid following keratanase II digestion. |
| T2 |
129-388 |
Sentence |
denotes |
A previously developed method for the structural fingerprinting of keratan sulfates (Brown et al., Glycobiology, 5, 311-317, 1995) has been adapted for use with oligosaccharides fluorescently labeled with 2-aminobenzoic acid following keratanase II digestion. |
| T2 |
129-388 |
Sentence |
denotes |
A previously developed method for the structural fingerprinting of keratan sulfates (Brown et al., Glycobiology, 5, 311-317, 1995) has been adapted for use with oligosaccharides fluorescently labeled with 2-aminobenzoic acid following keratanase II digestion. |
| TextSentencer_T3 |
389-492 |
Sentence |
denotes |
The oligosaccharides are separated by high-pH anion-exchange chromatography on a Dionex AS4A-SC column. |
| T3 |
389-492 |
Sentence |
denotes |
The oligosaccharides are separated by high-pH anion-exchange chromatography on a Dionex AS4A-SC column. |
| T3 |
389-492 |
Sentence |
denotes |
The oligosaccharides are separated by high-pH anion-exchange chromatography on a Dionex AS4A-SC column. |
| TextSentencer_T4 |
493-642 |
Sentence |
denotes |
This methodology permits quantitative analysis of labeled oligosaccharides which can be detected at the sub-nanogram ( approximately 100 fmol) level. |
| T4 |
493-642 |
Sentence |
denotes |
This methodology permits quantitative analysis of labeled oligosaccharides which can be detected at the sub-nanogram ( approximately 100 fmol) level. |
| T4 |
493-642 |
Sentence |
denotes |
This methodology permits quantitative analysis of labeled oligosaccharides which can be detected at the sub-nanogram ( approximately 100 fmol) level. |
| TextSentencer_T5 |
643-742 |
Sentence |
denotes |
Satisfactory calibration of this method can be achieved using commercial keratan sulfate standards. |
| T5 |
643-742 |
Sentence |
denotes |
Satisfactory calibration of this method can be achieved using commercial keratan sulfate standards. |
| T5 |
643-742 |
Sentence |
denotes |
Satisfactory calibration of this method can be achieved using commercial keratan sulfate standards. |
| TextSentencer_T6 |
743-902 |
Sentence |
denotes |
Keratan sulfates from porcine brain phosphocan and human ovarian tumors have been examined using this methodology, and their structural features are discussed. |
| T6 |
743-902 |
Sentence |
denotes |
Keratan sulfates from porcine brain phosphocan and human ovarian tumors have been examined using this methodology, and their structural features are discussed. |
| T6 |
743-902 |
Sentence |
denotes |
Keratan sulfates from porcine brain phosphocan and human ovarian tumors have been examined using this methodology, and their structural features are discussed. |