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PubMed:1671881 JSONTXT 49 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 49-64 DiseaseOrPhenotypicFeature denotes phenylketonuria
T2 66-91 DiseaseOrPhenotypicFeature denotes Classical phenylketonuria
T3 98-125 DiseaseOrPhenotypicFeature denotes autosomal recessive disease
T4 138-185 DiseaseOrPhenotypicFeature denotes deficiency of hepatic phenylalanine hydroxylase
T5 187-190 GeneOrGeneProduct denotes PAH
T6 272-275 GeneOrGeneProduct denotes PAH
T7 362-376 SequenceVariant denotes 272gly----stop
T8 381-394 SequenceVariant denotes 273ser----phe
T9 606-609 DiseaseOrPhenotypicFeature denotes PKU
T10 684-700 DiseaseOrPhenotypicFeature denotes PAH deficiencies