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PubMed:2793865 / 0-231 JSONTXT

Annnotations TAB JSON ListView MergeView

sentences

Id Subject Object Predicate Lexical cue
T1 0-106 Sentence denotes Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.
T1 0-106 Sentence denotes Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 139-152 HP_0001427 denotes mitochondrial

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
2793865-0#43#79#gene4942 43-79 gene4942 denotes ornithine aminotransferase precursor
2793865-0#91#105#diseaseC0018425 91-105 diseaseC0018425 denotes gyrate atrophy
2793865-1#82#85#gene4942 189-192 gene4942 denotes OAT
43#79#gene494291#105#diseaseC0018425 2793865-0#43#79#gene4942 2793865-0#91#105#diseaseC0018425 associated_with ornithine aminotransferase precursor,gyrate atrophy

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 91-105 Disease denotes gyrate atrophy http://purl.obolibrary.org/obo/MONDO_0009796
T2 189-192 Disease denotes OAT http://purl.obolibrary.org/obo/MONDO_0004483
T3 217-231 Disease denotes gyrate atrophy http://purl.obolibrary.org/obo/MONDO_0009796