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PubMed:10051572 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 625-645 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa 0008377|0019200
T3 647-649 DiseaseOrPhenotypicFeature denotes RP 0008377
T4 819-821 DiseaseOrPhenotypicFeature denotes RP 0008377
T5 1230-1232 DiseaseOrPhenotypicFeature denotes RP 0008377

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10051572-3#83#88#geners104893787 587-592 geners104893787 denotes C110Y
10051572-3#121#141#diseaseC0035334 625-645 diseaseC0035334 denotes retinitis pigmentosa
10051572-3#143#145#diseaseC0035334 647-649 diseaseC0035334 denotes RP
83#88#geners104893787121#141#diseaseC0035334 10051572-3#83#88#geners104893787 10051572-3#121#141#diseaseC0035334 associated_with C110Y,retinitis pigmentosa
83#88#geners104893787143#145#diseaseC0035334 10051572-3#83#88#geners104893787 10051572-3#143#145#diseaseC0035334 associated_with C110Y,RP

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10051572-8#53#62#gene6010 1255-1264 gene6010 denotes rhodopsin
10051572-8#28#30#diseaseC0035334 1230-1232 diseaseC0035334 denotes RP
53#62#gene601028#30#diseaseC0035334 10051572-8#53#62#gene6010 10051572-8#28#30#diseaseC0035334 associated_with rhodopsin,RP