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sentences

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.
TextSentencer_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.
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.
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.
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.
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.
T1 0-142 Sentence denotes Genetic analysis of a Japanese family with normotriglyceridemic abetalipoproteinemia indicates a lack of linkage to the apolipoprotein B gene.
T2 143-265 Sentence denotes Normotriglyceridemic abetalipoproteinemia is a rare familial disorder characterized by an isolated deficiency of 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.
T4 363-482 Sentence denotes To elucidate the genetic abnormalities in this family, we studied the linkage of apoB gene using three genetic markers.
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.
T6 652-758 Sentence denotes By contrast, an American case had a point substitution in the apoB gene generating an in-frame stop codon.
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.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 120-136 gene:338 denotes apolipoprotein B
T1 64-84 disease:C0000744 denotes abetalipoproteinemia
R1 T0 T1 associated_with apolipoprotein B,abetalipoproteinemia

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 164-184 HP_0008181 denotes abetalipoproteinemia

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 164-184 HP:0008181 denotes abetalipoproteinemia
TI1 64-84 HP:0008181 denotes abetalipoproteinemia

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 164-184 ORDO:14 denotes abetalipoproteinemia
TI1 64-84 ORDO:14 denotes abetalipoproteinemia

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 43-84 SpecificDisease:D000012 denotes normotriglyceridemic abetalipoproteinemia
T2 143-184 SpecificDisease:D000012 denotes Normotriglyceridemic abetalipoproteinemia
T3 195-212 DiseaseClass:D009358 denotes familial disorder
T4 242-264 SpecificDisease:OMIM:200100 denotes deficiency of apoB-100
T5 380-401 DiseaseClass:D030342 denotes genetic abnormalities

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T3092 43-84 SpecificDisease denotes normotriglyceridemic abetalipoproteinemia D000012
T3093 143-184 SpecificDisease denotes Normotriglyceridemic abetalipoproteinemia D000012
T3094 195-212 DiseaseClass denotes familial disorder D009358
T3095 242-264 SpecificDisease denotes deficiency of apoB-100 OMIM:200100
T3096 380-401 DiseaseClass denotes genetic abnormalities D030342

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T3092 43-84 SpecificDisease denotes normotriglyceridemic abetalipoproteinemia D000012
T3093 143-184 SpecificDisease denotes Normotriglyceridemic abetalipoproteinemia D000012
T3094 195-212 DiseaseClass denotes familial disorder D009358
T3095 242-264 SpecificDisease denotes deficiency of apoB-100 OMIM:200100
T3096 380-401 DiseaseClass denotes genetic abnormalities D030342

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 43-84 SpecificDisease denotes normotriglyceridemic abetalipoproteinemia
T2 143-184 SpecificDisease denotes Normotriglyceridemic abetalipoproteinemia
T3 314-321 DiseaseClass denotes disease
T4 627-635 DiseaseClass denotes disorder
T5 792-800 DiseaseClass denotes disorder

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 43-84 SpecificDisease denotes normotriglyceridemic abetalipoproteinemia
T2 143-184 SpecificDisease denotes Normotriglyceridemic abetalipoproteinemia
T3 314-321 DiseaseClass denotes disease
T4 627-635 DiseaseClass denotes disorder
T5 792-800 DiseaseClass denotes disorder

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 43-84 SpecificDisease denotes normotriglyceridemic abetalipoproteinemia
T2 143-184 SpecificDisease denotes Normotriglyceridemic abetalipoproteinemia
T3 622-635 Modifier denotes this disorder
T4 787-800 Modifier denotes this disorder

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 43-84 SpecificDisease denotes normotriglyceridemic abetalipoproteinemia
T2 143-184 SpecificDisease denotes Normotriglyceridemic abetalipoproteinemia
T3 309-321 SpecificDisease denotes this disease
T4 622-635 SpecificDisease denotes this disorder
T5 787-800 SpecificDisease denotes this disorder