| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-102 |
Sentence |
denotes |
Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia. |
| T1 |
0-102 |
Sentence |
denotes |
Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia. |
| T1 |
0-102 |
Sentence |
denotes |
Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia. |
| TextSentencer_T2 |
103-247 |
Sentence |
denotes |
The biochemical hallmark of Congenital Disorders of Glycosylation (CDG) including type Ia is a defective N-glycosylation of serum glycoproteins. |
| T2 |
103-247 |
Sentence |
denotes |
The biochemical hallmark of Congenital Disorders of Glycosylation (CDG) including type Ia is a defective N-glycosylation of serum glycoproteins. |
| T2 |
103-247 |
Sentence |
denotes |
The biochemical hallmark of Congenital Disorders of Glycosylation (CDG) including type Ia is a defective N-glycosylation of serum glycoproteins. |
| TextSentencer_T3 |
248-358 |
Sentence |
denotes |
Hypoglycosylated forms of alpha1-antitrypsin have been detected by Western blot in serum from CDG Ia patients. |
| T3 |
248-358 |
Sentence |
denotes |
Hypoglycosylated forms of alpha1-antitrypsin have been detected by Western blot in serum from CDG Ia patients. |
| T3 |
248-358 |
Sentence |
denotes |
Hypoglycosylated forms of alpha1-antitrypsin have been detected by Western blot in serum from CDG Ia patients. |
| TextSentencer_T4 |
359-509 |
Sentence |
denotes |
In contrast we were not able to detect hypoglycosylation in alpha1-antitrypsin synthesized by fibroblasts, keratinocytes, enterocytes, and leukocytes. |
| T4 |
359-509 |
Sentence |
denotes |
In contrast we were not able to detect hypoglycosylation in alpha1-antitrypsin synthesized by fibroblasts, keratinocytes, enterocytes, and leukocytes. |
| T4 |
359-509 |
Sentence |
denotes |
In contrast we were not able to detect hypoglycosylation in alpha1-antitrypsin synthesized by fibroblasts, keratinocytes, enterocytes, and leukocytes. |
| TextSentencer_T5 |
510-721 |
Sentence |
denotes |
Similarly no hypoglycosylation was detectable in a membrane-associated N-linked glycoprotein, the facilitative glucose transporter GLUT-1 and also in serum immunoglobulin G isolated from sera of CDG Ia patients. |
| T5 |
510-721 |
Sentence |
denotes |
Similarly no hypoglycosylation was detectable in a membrane-associated N-linked glycoprotein, the facilitative glucose transporter GLUT-1 and also in serum immunoglobulin G isolated from sera of CDG Ia patients. |
| T5 |
510-721 |
Sentence |
denotes |
Similarly no hypoglycosylation was detectable in a membrane-associated N-linked glycoprotein, the facilitative glucose transporter GLUT-1 and also in serum immunoglobulin G isolated from sera of CDG Ia patients. |
| TextSentencer_T6 |
722-795 |
Sentence |
denotes |
We conclude that the phenotypic expression of CDG Ia is tissue-dependent. |
| T6 |
722-795 |
Sentence |
denotes |
We conclude that the phenotypic expression of CDG Ia is tissue-dependent. |
| T6 |
722-795 |
Sentence |
denotes |
We conclude that the phenotypic expression of CDG Ia is tissue-dependent. |