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PubMed:17671735 JSONTXT 42 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 66-74 OrganismTaxon denotes patients
T2 93-97 GeneOrGeneProduct denotes GJB2
T3 154-186 DiseaseOrPhenotypicFeature denotes sensorineural hearing impairment
T4 405-423 DiseaseOrPhenotypicFeature denotes hearing impairment
T5 461-465 GeneOrGeneProduct denotes GJB2
T6 516-520 GeneOrGeneProduct denotes GJB2
T7 527-535 OrganismTaxon denotes patients
T8 541-559 DiseaseOrPhenotypicFeature denotes hearing impairment
T9 607-611 GeneOrGeneProduct denotes GJB6
T10 616-620 GeneOrGeneProduct denotes GJB3
T11 657-661 GeneOrGeneProduct denotes GJB2
T12 707-711 GeneOrGeneProduct denotes GJB2
T13 725-733 OrganismTaxon denotes patients
T14 776-784 SequenceVariant denotes -3170G>A
T15 808-812 GeneOrGeneProduct denotes GJB2
T16 834-842 OrganismTaxon denotes patients
T17 861-869 SequenceVariant denotes -3170G>A
T18 899-906 SequenceVariant denotes p.R127H
T19 920-924 GeneOrGeneProduct denotes GJB2
T20 967-971 GeneOrGeneProduct denotes GJB6
T21 979-983 GeneOrGeneProduct denotes GJB6
T22 1047-1051 GeneOrGeneProduct denotes GJB3
T23 1053-1061 SequenceVariant denotes c.357C>T
T24 1063-1071 SequenceVariant denotes c.798C>T
T25 1076-1083 SequenceVariant denotes c.94C>T
T26 1085-1091 SequenceVariant denotes p.R32W
T27 1210-1218 SequenceVariant denotes -3170G>A
T28 1244-1252 SequenceVariant denotes c.35delG
T29 1257-1265 OrganismTaxon denotes patients
T30 1271-1289 DiseaseOrPhenotypicFeature denotes hearing impairment