Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-88 |
Sentence |
denotes |
Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene. |
T1 |
0-88 |
Sentence |
denotes |
Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene. |
TextSentencer_T2 |
89-100 |
Sentence |
denotes |
BACKGROUND: |
T2 |
89-100 |
Sentence |
denotes |
BACKGROUND: |
TextSentencer_T3 |
101-407 |
Sentence |
denotes |
Although apolipoprotein A-II (apoA-II) associated amyloidosis has been described in the senescent accelerated mouse (SAM) model of aging, so far there has been no report of human apoA-II amyloidosis except for a recent report of renal amyloidosis resulting from a stop-codon to glycine mutation of apoA-II. |
T3 |
101-407 |
Sentence |
denotes |
Although apolipoprotein A-II (apoA-II) associated amyloidosis has been described in the senescent accelerated mouse (SAM) model of aging, so far there has been no report of human apoA-II amyloidosis except for a recent report of renal amyloidosis resulting from a stop-codon to glycine mutation of apoA-II. |
TextSentencer_T4 |
408-487 |
Sentence |
denotes |
The mechanisms of amyloid formation in human apoA-II amyloidosis are not clear. |
T4 |
408-487 |
Sentence |
denotes |
The mechanisms of amyloid formation in human apoA-II amyloidosis are not clear. |
TextSentencer_T5 |
488-496 |
Sentence |
denotes |
METHODS: |
T5 |
488-496 |
Sentence |
denotes |
METHODS: |
TextSentencer_T6 |
497-580 |
Sentence |
denotes |
A 46-year-old Caucasian male with proteinuria noted at 42 years of age was studied. |
T6 |
497-580 |
Sentence |
denotes |
A 46-year-old Caucasian male with proteinuria noted at 42 years of age was studied. |
TextSentencer_T7 |
581-635 |
Sentence |
denotes |
Renal biopsy revealed amyloid deposition in glomeruli. |
T7 |
581-635 |
Sentence |
denotes |
Renal biopsy revealed amyloid deposition in glomeruli. |
TextSentencer_T8 |
636-741 |
Sentence |
denotes |
DNA analysis of genes known to be associated with hereditary renal amyloidosis revealed no abnormalities. |
T8 |
636-741 |
Sentence |
denotes |
DNA analysis of genes known to be associated with hereditary renal amyloidosis revealed no abnormalities. |
TextSentencer_T9 |
742-830 |
Sentence |
denotes |
To elucidate the type of his amyloidosis, apoA-II gene and plasma apoA-II were examined. |
T9 |
742-830 |
Sentence |
denotes |
To elucidate the type of his amyloidosis, apoA-II gene and plasma apoA-II were examined. |
TextSentencer_T10 |
831-1014 |
Sentence |
denotes |
RESULTS: DNA analysis revealed heterozygosity for a G to C transversion at the second position of the stop-codon of apoA-II gene, suggesting a stop to serine substitution at codon 78. |
T10 |
831-1014 |
Sentence |
denotes |
RESULTS: DNA analysis revealed heterozygosity for a G to C transversion at the second position of the stop-codon of apoA-II gene, suggesting a stop to serine substitution at codon 78. |
TextSentencer_T11 |
1015-1206 |
Sentence |
denotes |
Western blot analysis and amino acid sequence analysis of the patient's plasma apoA-II showed both normal apoA-II and variant apoA-II with a 21-amino acid residue extension at the C-terminus. |
T11 |
1015-1206 |
Sentence |
denotes |
Western blot analysis and amino acid sequence analysis of the patient's plasma apoA-II showed both normal apoA-II and variant apoA-II with a 21-amino acid residue extension at the C-terminus. |
TextSentencer_T12 |
1207-1219 |
Sentence |
denotes |
CONCLUSIONS: |
T12 |
1207-1219 |
Sentence |
denotes |
CONCLUSIONS: |
TextSentencer_T13 |
1220-1421 |
Sentence |
denotes |
These results indicate that the patient's amyloid fibrils were derived from apoA-II and the amyloidogenesis is likely to be closely linked to the peptide extension at the C-terminus of variant apoA-II. |
T13 |
1220-1421 |
Sentence |
denotes |
These results indicate that the patient's amyloid fibrils were derived from apoA-II and the amyloidogenesis is likely to be closely linked to the peptide extension at the C-terminus of variant apoA-II. |
TextSentencer_T14 |
1422-1498 |
Sentence |
denotes |
The pathogenesis of human apoA-II amyloidosis is different from that of SAM. |
T14 |
1422-1498 |
Sentence |
denotes |
The pathogenesis of human apoA-II amyloidosis is different from that of SAM. |