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PubMed:10567373 / 122-173 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T1 0-51 disease:C2931834 denotes persistent hyperinsulinemic hypoglycemia of infancy
T3 0-51 disease:C2931833 denotes persistent hyperinsulinemic hypoglycemia of infancy
T5 0-51 disease:C0027773 denotes persistent hyperinsulinemic hypoglycemia of infancy
T7 0-51 disease:C2931834 denotes persistent hyperinsulinemic hypoglycemia of infancy
T9 0-51 disease:C2931833 denotes persistent hyperinsulinemic hypoglycemia of infancy
T11 0-51 disease:C0027773 denotes persistent hyperinsulinemic hypoglycemia of infancy

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 0-51 Disease denotes persistent hyperinsulinemic hypoglycemia of infancy http://purl.obolibrary.org/obo/MONDO_0009734|http://purl.obolibrary.org/obo/MONDO_0011153|http://purl.obolibrary.org/obo/MONDO_0019010

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T1 11-40 Phenotype denotes hyperinsulinemic hypoglycemia HP:0000825