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PubMed:37981655 JSONTXT

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mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 22-27 Disease denotes USH2A http://purl.obolibrary.org/obo/MONDO_0010169
T2 263-284 Disease denotes Usher syndrome type 2 http://purl.obolibrary.org/obo/MONDO_0016484
T3 286-290 Disease denotes USH2 http://purl.obolibrary.org/obo/MONDO_0016484
T4 309-314 Disease denotes USH2A http://purl.obolibrary.org/obo/MONDO_0010169
T5 431-436 Disease denotes USH2A http://purl.obolibrary.org/obo/MONDO_0010169
T6 666-671 Disease denotes USH2A http://purl.obolibrary.org/obo/MONDO_0010169
T7 752-764 Disease denotes hearing loss http://purl.obolibrary.org/obo/MONDO_0005365
T8 1024-1044 Disease denotes retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0008377|http://purl.obolibrary.org/obo/MONDO_0019200
T10 1109-1114 Disease denotes USH2A http://purl.obolibrary.org/obo/MONDO_0010169
T11 1123-1127 Disease denotes USH2 http://purl.obolibrary.org/obo/MONDO_0016484
T12 1138-1163 Disease denotes nonsyndromic hearing loss http://purl.obolibrary.org/obo/MONDO_0019497
T13 1347-1352 Disease denotes USH2A http://purl.obolibrary.org/obo/MONDO_0010169

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 752-764 Phenotype denotes hearing loss HP:0000365
T2 1024-1044 Phenotype denotes retinitis pigmentosa HP:0000510
T3 1151-1163 Phenotype denotes hearing loss HP:0000365