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PubMed:2563166 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 137-147 gene:338 denotes apo) B-100
T1 153-168 disease:C0019247 denotes genetic disease
T2 137-147 gene:338 denotes apo) B-100
T3 183-203 disease:C0020443 denotes hypercholesterolemia
T4 308-321 gene:3949 denotes LDL) receptor
T5 153-168 disease:C0019247 denotes genetic disease
T6 308-321 gene:3949 denotes LDL) receptor
T7 183-203 disease:C0020443 denotes hypercholesterolemia
R1 T0 T1 associated_with apo) B-100,genetic disease
R2 T2 T3 associated_with apo) B-100,hypercholesterolemia
R3 T4 T5 associated_with LDL) receptor,genetic disease
R4 T6 T7 associated_with LDL) receptor,hypercholesterolemia

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 183-203 HP_0003124 denotes hypercholesterolemia
T2 1318-1338 HP_0003124 denotes hypercholesterolemia

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
2563166-0#31#47#gene338 31-47 gene338 denotes apolipoprotein B
2563166-0#61#100#diseaseC1704417 61-100 diseaseC1704417 denotes familial defective apolipoprotein B-100
2563166-1#206#219#gene3949 308-321 gene3949 denotes LDL) receptor
2563166-1#81#101#diseaseC0020443 183-203 diseaseC0020443 denotes hypercholesterolemia
2563166-7#126#134#gene338 1245-1253 gene338 denotes r apoB-1
2563166-7#197#217#diseaseC0020443 1316-1336 diseaseC0020443 denotes d hypercholesterolem
31#47#gene33861#100#diseaseC1704417 2563166-0#31#47#gene338 2563166-0#61#100#diseaseC1704417 associated_with apolipoprotein B,familial defective apolipoprotein B-100
206#219#gene394981#101#diseaseC0020443 2563166-1#206#219#gene3949 2563166-1#81#101#diseaseC0020443 associated_with LDL) receptor,hypercholesterolemia
126#134#gene338197#217#diseaseC0020443 2563166-7#126#134#gene338 2563166-7#197#217#diseaseC0020443 associated_with r apoB-1,d hypercholesterolem