| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-122 |
Sentence |
denotes |
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups. |
| T1 |
0-122 |
Sentence |
denotes |
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups. |
| T1 |
0-122 |
Sentence |
denotes |
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups. |
| TextSentencer_T2 |
123-279 |
Sentence |
denotes |
Defects in the biosynthesis of N- and core 1 O-glycans may be found by isoelectric focusing (IEF) of plasma transferrin and apolipoprotein C-III (apoC-III). |
| T2 |
123-279 |
Sentence |
denotes |
Defects in the biosynthesis of N- and core 1 O-glycans may be found by isoelectric focusing (IEF) of plasma transferrin and apolipoprotein C-III (apoC-III). |
| T2 |
123-279 |
Sentence |
denotes |
Defects in the biosynthesis of N- and core 1 O-glycans may be found by isoelectric focusing (IEF) of plasma transferrin and apolipoprotein C-III (apoC-III). |
| TextSentencer_T3 |
280-521 |
Sentence |
denotes |
We hypothesized that IEF of transferrin and apoC-III in combination with sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) of apoC-III may provide a classification for congenital disorders of glycosylation (CDG) patients. |
| T3 |
280-521 |
Sentence |
denotes |
We hypothesized that IEF of transferrin and apoC-III in combination with sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) of apoC-III may provide a classification for congenital disorders of glycosylation (CDG) patients. |
| T3 |
280-521 |
Sentence |
denotes |
We hypothesized that IEF of transferrin and apoC-III in combination with sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) of apoC-III may provide a classification for congenital disorders of glycosylation (CDG) patients. |
| TextSentencer_T4 |
522-646 |
Sentence |
denotes |
We analyzed plasma from 22 patients with eight different and well-characterized CDG subtypes and 19 cases with unsolved CDG. |
| T4 |
522-646 |
Sentence |
denotes |
We analyzed plasma from 22 patients with eight different and well-characterized CDG subtypes and 19 cases with unsolved CDG. |
| T4 |
522-646 |
Sentence |
denotes |
We analyzed plasma from 22 patients with eight different and well-characterized CDG subtypes and 19 cases with unsolved CDG. |
| TextSentencer_T5 |
647-782 |
Sentence |
denotes |
Transferrin IEF (TIEF) has been used to distinguish between N-glycan assembly (type 1 profile) and processing (type 2 profile) defects. |
| T5 |
647-782 |
Sentence |
denotes |
Transferrin IEF (TIEF) has been used to distinguish between N-glycan assembly (type 1 profile) and processing (type 2 profile) defects. |
| T5 |
647-782 |
Sentence |
denotes |
Transferrin IEF (TIEF) has been used to distinguish between N-glycan assembly (type 1 profile) and processing (type 2 profile) defects. |
| TextSentencer_T6 |
783-840 |
Sentence |
denotes |
We differentiated two different CDG type 2 TIEF profiles: |
| T6 |
783-840 |
Sentence |
denotes |
We differentiated two different CDG type 2 TIEF profiles: |
| T6 |
783-840 |
Sentence |
denotes |
We differentiated two different CDG type 2 TIEF profiles: |
| TextSentencer_T7 |
841-1027 |
Sentence |
denotes |
The "asialo profile" characterized by elevated levels of asialo- and monosialotransferrin and the "disialo profile" characterized by increased levels of disialo- and trisialotransferrin. |
| T7 |
841-1027 |
Sentence |
denotes |
The "asialo profile" characterized by elevated levels of asialo- and monosialotransferrin and the "disialo profile" characterized by increased levels of disialo- and trisialotransferrin. |
| T7 |
841-1027 |
Sentence |
denotes |
The "asialo profile" characterized by elevated levels of asialo- and monosialotransferrin and the "disialo profile" characterized by increased levels of disialo- and trisialotransferrin. |
| TextSentencer_T8 |
1028-1111 |
Sentence |
denotes |
ApoC-III IEF gave two abnormal profiles ("apoC-III(0)" and "apoC-III(1)" profiles). |
| T8 |
1028-1111 |
Sentence |
denotes |
ApoC-III IEF gave two abnormal profiles ("apoC-III(0)" and "apoC-III(1)" profiles). |
| T8 |
1028-1111 |
Sentence |
denotes |
ApoC-III IEF gave two abnormal profiles ("apoC-III(0)" and "apoC-III(1)" profiles). |
| TextSentencer_T9 |
1112-1252 |
Sentence |
denotes |
The results for the eight established CDG forms exactly matched the theoretical expectations, providing a validation for the study approach. |
| T9 |
1112-1252 |
Sentence |
denotes |
The results for the eight established CDG forms exactly matched the theoretical expectations, providing a validation for the study approach. |
| T9 |
1112-1252 |
Sentence |
denotes |
The results for the eight established CDG forms exactly matched the theoretical expectations, providing a validation for the study approach. |
| TextSentencer_T10 |
1253-1407 |
Sentence |
denotes |
The combination of the three electrophoretic techniques was not additionally informative for the CDG-Ix patients as they had normal apoC-III IEF patterns. |
| T10 |
1253-1407 |
Sentence |
denotes |
The combination of the three electrophoretic techniques was not additionally informative for the CDG-Ix patients as they had normal apoC-III IEF patterns. |
| T10 |
1253-1407 |
Sentence |
denotes |
The combination of the three electrophoretic techniques was not additionally informative for the CDG-Ix patients as they had normal apoC-III IEF patterns. |
| TextSentencer_T11 |
1408-1497 |
Sentence |
denotes |
However, the CDG-IIx patients could be further subdivided into six biochemical subgroups. |
| T11 |
1408-1497 |
Sentence |
denotes |
However, the CDG-IIx patients could be further subdivided into six biochemical subgroups. |
| T11 |
1408-1497 |
Sentence |
denotes |
However, the CDG-IIx patients could be further subdivided into six biochemical subgroups. |
| TextSentencer_T12 |
1498-1736 |
Sentence |
denotes |
The robustness of the methodology was supported by the fact that three patients with similar clinical features ended in the same subgroup and that another patient, classified in the "CDG-IIe subgroup," turned out to have a similar defect. |
| T12 |
1498-1736 |
Sentence |
denotes |
The robustness of the methodology was supported by the fact that three patients with similar clinical features ended in the same subgroup and that another patient, classified in the "CDG-IIe subgroup," turned out to have a similar defect. |
| T12 |
1498-1736 |
Sentence |
denotes |
The robustness of the methodology was supported by the fact that three patients with similar clinical features ended in the same subgroup and that another patient, classified in the "CDG-IIe subgroup," turned out to have a similar defect. |
| TextSentencer_T13 |
1737-1922 |
Sentence |
denotes |
Dividing the CDG-IIx patients in six subgroups narrows down drastically the options of the primary defect in each of the subgroups and will be helpful to define new CDG type II defects. |
| T13 |
1737-1922 |
Sentence |
denotes |
Dividing the CDG-IIx patients in six subgroups narrows down drastically the options of the primary defect in each of the subgroups and will be helpful to define new CDG type II defects. |
| T13 |
1737-1922 |
Sentence |
denotes |
Dividing the CDG-IIx patients in six subgroups narrows down drastically the options of the primary defect in each of the subgroups and will be helpful to define new CDG type II defects. |