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PubMed:1347103 JSONTXT

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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
1347103-1#258#270#gene3949 345-357 gene3949 denotes LDL receptor
1347103-1#0#39#diseaseC1704417 87-126 diseaseC1704417 denotes Familial defective apolipoprotein B-100
1347103-1#41#44#diseaseC1704417 128-131 diseaseC1704417 denotes FDB
1347103-1#52#79#diseaseC3899989 139-166 diseaseC3899989 denotes autosomal dominant disorder
1347103-1#96#117#diseaseC0020443 183-204 diseaseC0020443 denotes hypercholesterolaemia
258#270#gene39490#39#diseaseC1704417 1347103-1#258#270#gene3949 1347103-1#0#39#diseaseC1704417 associated_with LDL receptor,Familial defective apolipoprotein B-100
258#270#gene394941#44#diseaseC1704417 1347103-1#258#270#gene3949 1347103-1#41#44#diseaseC1704417 associated_with LDL receptor,FDB
258#270#gene394952#79#diseaseC3899989 1347103-1#258#270#gene3949 1347103-1#52#79#diseaseC3899989 associated_with LDL receptor,autosomal dominant disorder
258#270#gene394996#117#diseaseC0020443 1347103-1#258#270#gene3949 1347103-1#96#117#diseaseC0020443 associated_with LDL receptor,hypercholesterolaemia

DisGeNET

Id Subject Object Predicate Lexical cue
T0 345-357 gene:3949 denotes LDL receptor
T1 87-126 disease:C1704417 denotes Familial defective apolipoprotein B-100
T2 345-357 gene:3949 denotes LDL receptor
T3 128-131 disease:C1704417 denotes FDB
T4 345-357 gene:3949 denotes LDL receptor
T5 183-204 disease:C0020443 denotes hypercholesterolaemia
R1 T0 T1 associated_with LDL receptor,Familial defective apolipoprotein B-100
R2 T2 T3 associated_with LDL receptor,FDB
R3 T4 T5 associated_with LDL receptor,hypercholesterolaemia