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PubMed:11574907 JSONTXT 7 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue mondo_id
T1 91-114 DiseaseOrPhenotypicFeature denotes oculocutaneous albinism 0018910
T2 116-120 DiseaseOrPhenotypicFeature denotes OCA4 0011683
T3 122-145 DiseaseOrPhenotypicFeature denotes Oculocutaneous albinism 0018910
T4 147-150 DiseaseOrPhenotypicFeature denotes OCA 0018910
T5 214-217 DiseaseOrPhenotypicFeature denotes OCA 0018910
T6 238-254 DiseaseOrPhenotypicFeature denotes hypopigmentation 0007459
T7 343-352 DiseaseOrPhenotypicFeature denotes nystagmus 0005712
T8 366-376 DiseaseOrPhenotypicFeature denotes strabismus 0003432
T9 433-437 DiseaseOrPhenotypicFeature denotes skin 0002531
T10 469-480 DiseaseOrPhenotypicFeature denotes skin cancer 0002898
T11 526-529 DiseaseOrPhenotypicFeature denotes OCA 0018910
T12 551-555 DiseaseOrPhenotypicFeature denotes OCA1 0018135
T13 736-739 DiseaseOrPhenotypicFeature denotes OCA 0018910
T14 751-755 DiseaseOrPhenotypicFeature denotes OCA2 0008746
T15 794-797 DiseaseOrPhenotypicFeature denotes OCA 0018910
T16 880-883 DiseaseOrPhenotypicFeature denotes OCA 0018910
T17 895-899 DiseaseOrPhenotypicFeature denotes OCA3 0008747
T18 929-932 DiseaseOrPhenotypicFeature denotes OCA 0018910
T19 963-971 DiseaseOrPhenotypicFeature denotes albinism 0043209
T20 1102-1105 DiseaseOrPhenotypicFeature denotes OCA 0018910
T21 1155-1158 DiseaseOrPhenotypicFeature denotes OCA 0018910
T22 1272-1275 DiseaseOrPhenotypicFeature denotes OCA 0018910
T23 1285-1289 DiseaseOrPhenotypicFeature denotes OCA4 0011683