| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-100 |
Sentence |
denotes |
A case of Werner syndrome without metabolic abnormality: implications for the early pathophysiology. |
| T1 |
0-100 |
Sentence |
denotes |
A case of Werner syndrome without metabolic abnormality: implications for the early pathophysiology. |
| TextSentencer_T2 |
101-211 |
Sentence |
denotes |
Werner syndrome (WS) is an autosomal recessive progeroid disorder caused by mutations in the WRN DNA helicase. |
| T2 |
101-211 |
Sentence |
denotes |
Werner syndrome (WS) is an autosomal recessive progeroid disorder caused by mutations in the WRN DNA helicase. |
| TextSentencer_T3 |
212-445 |
Sentence |
denotes |
It is characterized by the graying and loss of hair, juvenile cataracts, sclerosis and ulceration of skin, insulin-resistant diabetes mellitus, dyslipidemia, abdominal adiposity, osteoporosis, atherosclerosis, and malignant neoplasm. |
| T3 |
212-445 |
Sentence |
denotes |
It is characterized by the graying and loss of hair, juvenile cataracts, sclerosis and ulceration of skin, insulin-resistant diabetes mellitus, dyslipidemia, abdominal adiposity, osteoporosis, atherosclerosis, and malignant neoplasm. |
| TextSentencer_T4 |
446-574 |
Sentence |
denotes |
Patients are usually diagnosed in their 30s or 40s, but the early pathophysiology of the syndrome is still not fully understood. |
| T4 |
446-574 |
Sentence |
denotes |
Patients are usually diagnosed in their 30s or 40s, but the early pathophysiology of the syndrome is still not fully understood. |
| TextSentencer_T5 |
575-683 |
Sentence |
denotes |
Here we report a 29-year-old female patient who displayed cataracts, hair graying, and tendinous calcinosis. |
| T5 |
575-683 |
Sentence |
denotes |
Here we report a 29-year-old female patient who displayed cataracts, hair graying, and tendinous calcinosis. |
| TextSentencer_T6 |
684-715 |
Sentence |
denotes |
Her parents were first cousins. |
| T6 |
684-715 |
Sentence |
denotes |
Her parents were first cousins. |
| TextSentencer_T7 |
716-861 |
Sentence |
denotes |
Interestingly, the patient lacked the metabolic signs typical for WS, including glucose intolerance, dyslipidemia, and visceral fat accumulation. |
| T7 |
716-861 |
Sentence |
denotes |
Interestingly, the patient lacked the metabolic signs typical for WS, including glucose intolerance, dyslipidemia, and visceral fat accumulation. |
| TextSentencer_T8 |
862-947 |
Sentence |
denotes |
A hyperinsulinemic response at 30 min was observed in an oral glucose tolerance test. |
| T8 |
862-947 |
Sentence |
denotes |
A hyperinsulinemic response at 30 min was observed in an oral glucose tolerance test. |
| TextSentencer_T9 |
948-1171 |
Sentence |
denotes |
Mutational analysis for the WRN gene revealed a homozygous nucleotide substitution 3190C>T in exon 24, resulting in a protein product with replacement of an arginine residue at position 573 by termination codon (Arg987Ter). |
| T9 |
948-1171 |
Sentence |
denotes |
Mutational analysis for the WRN gene revealed a homozygous nucleotide substitution 3190C>T in exon 24, resulting in a protein product with replacement of an arginine residue at position 573 by termination codon (Arg987Ter). |
| TextSentencer_T10 |
1172-1265 |
Sentence |
denotes |
The mutated WRN protein was unable to translocate into the nucleus in an in vitro cell assay. |
| T10 |
1172-1265 |
Sentence |
denotes |
The mutated WRN protein was unable to translocate into the nucleus in an in vitro cell assay. |
| TextSentencer_T11 |
1266-1406 |
Sentence |
denotes |
A WS patient with an Arg987Ter mutation has been previously reported in Switzerland, the present case is the first to be identified in Asia. |
| T11 |
1266-1406 |
Sentence |
denotes |
A WS patient with an Arg987Ter mutation has been previously reported in Switzerland, the present case is the first to be identified in Asia. |
| TextSentencer_T12 |
1407-1588 |
Sentence |
denotes |
This case demonstrates the early clinical features of WS and suggests that metabolic abnormality, including insulin resistance, is not an essential component of WS at disease onset. |
| T12 |
1407-1588 |
Sentence |
denotes |
This case demonstrates the early clinical features of WS and suggests that metabolic abnormality, including insulin resistance, is not an essential component of WS at disease onset. |
| TextSentencer_T13 |
1589-1736 |
Sentence |
denotes |
Moreover, a follow-up study of such case would be useful to understand how the various clinical symptoms in WS develop and progress over the years. |
| T13 |
1589-1736 |
Sentence |
denotes |
Moreover, a follow-up study of such case would be useful to understand how the various clinical symptoms in WS develop and progress over the years. |