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PubMed:10090887 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 176-193 DiseaseOrPhenotypicFeature denotes Stargardt disease 0019353
T2 232-249 DiseaseOrPhenotypicFeature denotes Stargardt disease 0019353
T3 251-255 DiseaseOrPhenotypicFeature denotes STGD 0019353
T4 689-693 DiseaseOrPhenotypicFeature denotes STGD 0019353
T5 916-920 DiseaseOrPhenotypicFeature denotes STGD 0019353
T6 1054-1058 DiseaseOrPhenotypicFeature denotes STGD 0019353
T7 1162-1166 DiseaseOrPhenotypicFeature denotes STGD 0019353
T8 1333-1348 DiseaseOrPhenotypicFeature denotes cystic fibrosis 0009061
T9 1407-1411 DiseaseOrPhenotypicFeature denotes STGD 0019353
T10 1572-1576 DiseaseOrPhenotypicFeature denotes STGD 0019353

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10090887-7#4#13#geners76157638 1181-1190 geners76157638 denotes 2588G-->C
10090887-7#156#171#diseaseC0010674 1333-1348 diseaseC0010674 denotes cystic fibrosis
10090887-8#58#67#geners76157638 1456-1465 geners76157638 denotes 2588G-->C
10090887-8#174#178#diseaseC1855465 1572-1576 diseaseC1855465 denotes STGD
4#13#geners76157638156#171#diseaseC0010674 10090887-7#4#13#geners76157638 10090887-7#156#171#diseaseC0010674 associated_with 2588G-->C,cystic fibrosis
58#67#geners76157638174#178#diseaseC1855465 10090887-8#58#67#geners76157638 10090887-8#174#178#diseaseC1855465 associated_with 2588G-->C,STGD

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10090887-8#128#132#gene24 1526-1530 gene24 denotes ABCR
10090887-8#174#178#diseaseC1855465 1572-1576 diseaseC1855465 denotes STGD
128#132#gene24174#178#diseaseC1855465 10090887-8#128#132#gene24 10090887-8#174#178#diseaseC1855465 associated_with ABCR,STGD

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1526-1530 gene:24 denotes ABCR
T1 1572-1576 disease:C1855465 denotes STGD
R1 T0 T1 associated_with ABCR,STGD

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 1292-1318 HP_0000007 denotes severe autosomal recessive
T2 1299-1318 HP_0000007 denotes autosomal recessive