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PubMed:39277603 JSONTXT

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mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 32-53 Disease denotes retinal degenerations http://purl.obolibrary.org/obo/MONDO_0004580
T2 67-70 Disease denotes IRD http://purl.obolibrary.org/obo/MONDO_0019174
T3 83-112 Disease denotes Inherited retinal dystrophies http://purl.obolibrary.org/obo/MONDO_0019118
T4 128-132 Disease denotes IRDs http://purl.obolibrary.org/obo/MONDO_0009971
T5 159-176 Disease denotes visual impairment http://purl.obolibrary.org/obo/MONDO_0001941
T6 200-209 Disease denotes blindness http://purl.obolibrary.org/obo/MONDO_0001941
T7 457-461 Disease denotes IRDs http://purl.obolibrary.org/obo/MONDO_0009971
T8 529-532 Disease denotes HCP http://purl.obolibrary.org/obo/MONDO_0007369
T9 598-601 Disease denotes IRD http://purl.obolibrary.org/obo/MONDO_0019174
T10 777-780 Disease denotes IRD http://purl.obolibrary.org/obo/MONDO_0019174
T11 910-940 Disease denotes syndromic retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0020240
T12 1023-1026 Disease denotes IRD http://purl.obolibrary.org/obo/MONDO_0019174
T13 1037-1040 Disease denotes IRD http://purl.obolibrary.org/obo/MONDO_0019174
T14 1554-1557 Disease denotes IRD http://purl.obolibrary.org/obo/MONDO_0019174
T15 1601-1604 Disease denotes IRD http://purl.obolibrary.org/obo/MONDO_0019174

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 32-53 Phenotype denotes retinal degenerations HP:0000546
T2 93-112 Phenotype denotes retinal dystrophies HP:0000556
T3 159-176 Phenotype denotes visual impairment HP:0000505
T4 200-209 Phenotype denotes blindness HP:0000618
T5 920-940 Phenotype denotes retinitis pigmentosa HP:0000510

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 1013-1016 Body_part denotes web http://purl.obolibrary.org/obo/UBERON_0006015