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PubMed:10090896 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 54-75 DiseaseOrPhenotypicFeature denotes familial dysautonomia 0009131
T2 107-128 DiseaseOrPhenotypicFeature denotes Familial dysautonomia 0009131
T3 130-132 DiseaseOrPhenotypicFeature denotes FD 0009131
T4 726-728 DiseaseOrPhenotypicFeature denotes FD 0009131
T5 829-831 DiseaseOrPhenotypicFeature denotes FD 0009131
T6 911-913 DiseaseOrPhenotypicFeature denotes FD 0009131
T7 1089-1091 DiseaseOrPhenotypicFeature denotes FD 0009131
T8 1116-1118 DiseaseOrPhenotypicFeature denotes FD 0009131
T9 1235-1237 DiseaseOrPhenotypicFeature denotes FD 0009131
T10 1332-1334 DiseaseOrPhenotypicFeature denotes FD 0009131

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 116-128 HP_0002459 denotes dysautonomia
T2 140-159 HP_0000007 denotes autosomal recessive
T3 186-206 HP_0007281 denotes developmental arrest