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PubMed:1731805 JSONTXT 17 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-142 Sentence denotes Genetic analysis of a Japanese family with normotriglyceridemic abetalipoproteinemia indicates a lack of linkage to the apolipoprotein B gene.
T1 0-142 Sentence denotes Genetic analysis of a Japanese family with normotriglyceridemic abetalipoproteinemia indicates a lack of linkage to the apolipoprotein B gene.
TextSentencer_T2 143-265 Sentence denotes Normotriglyceridemic abetalipoproteinemia is a rare familial disorder characterized by an isolated deficiency of apoB-100.
T2 143-265 Sentence denotes Normotriglyceridemic abetalipoproteinemia is a rare familial disorder characterized by an isolated deficiency of apoB-100.
TextSentencer_T3 266-362 Sentence denotes We have previously reported a patient with this disease, who had normal apoB-48 but no apoB-100.
T3 266-362 Sentence denotes We have previously reported a patient with this disease, who had normal apoB-48 but no apoB-100.
TextSentencer_T4 363-482 Sentence denotes To elucidate the genetic abnormalities in this family, we studied the linkage of apoB gene using three genetic markers.
T4 363-482 Sentence denotes To elucidate the genetic abnormalities in this family, we studied the linkage of apoB gene using three genetic markers.
TextSentencer_T5 483-651 Sentence denotes The proband and her affected brother showed completely different apoB gene alleles, suggesting that the apoB gene itself is not related to this disorder in this family.
T5 483-651 Sentence denotes The proband and her affected brother showed completely different apoB gene alleles, suggesting that the apoB gene itself is not related to this disorder in this family.
TextSentencer_T6 652-758 Sentence denotes By contrast, an American case had a point substitution in the apoB gene generating an in-frame stop codon.
T6 652-758 Sentence denotes By contrast, an American case had a point substitution in the apoB gene generating an in-frame stop codon.
TextSentencer_T7 759-866 Sentence denotes These results indicate that this disorder can be caused by defect(s) of either an apoB gene or other genes.
T7 759-866 Sentence denotes These results indicate that this disorder can be caused by defect(s) of either an apoB gene or other genes.