> top > docs > PubMed:10051003 > annotations

PubMed:10051003 JSONTXT

Annnotations TAB JSON ListView MergeView

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 59-77 HP_0000006 denotes autosomal dominant
T2 163-185 HP_0000377 denotes external ear anomalies
T3 163-185 HP_0000356 denotes external ear anomalies
T4 163-185 HP_0008572 denotes external ear anomalies
T5 172-185 HP_0000598 denotes ear anomalies
T6 172-185 HP_0000356 denotes ear anomalies
T7 187-199 HP_0000365 denotes hearing loss
T8 201-221 HP_0100258 denotes preaxial polydactyly
T9 210-221 HP_0010442 denotes polydactyly
T10 210-246 HP_0001177 denotes polydactyly and triphalangeal thumbs
T11 226-246 HP_0001199 denotes triphalangeal thumbs
T12 270-289 HP_0012210 denotes renal malformations
T13 270-289 HP_0000077 denotes renal malformations
T14 368-386 HP_0001249 denotes mental retardation

BioLarkPubmedHPO

Id Subject Object Predicate Lexical cue
HP:0000006 59-77 HP:0000006 denotes autosomal dominant
HP:0003828 119-138 HP:0003828 denotes variable expression
HP:0000356 163-185 HP:0000356 denotes external ear anomalies
HP:0000365 187-199 HP:0000365 denotes hearing loss
HP:0001841 201-221 HP:0001841 denotes preaxial polydactyly
HP:0001177 201-221 HP:0001177 denotes preaxial polydactyly
HP:0001199 226-246 HP:0001199 denotes triphalangeal thumbs
HP:0002023 248-264 HP:0002023 denotes imperforate anus
HP:0000792 270-289 HP:0000792 denotes renal malformations
HP:0001249 368-386 HP:0001249 denotes mental retardation
T1 59-77 HP:0000006 denotes autosomal dominant
T2 119-138 HP:0003828 denotes variable expression
T3 163-185 HP:0000356 denotes external ear anomalies
T4 187-199 HP:0000365 denotes hearing loss
T5 201-221 HP:0001841 denotes preaxial polydactyly
T6 201-221 HP:0001177 denotes preaxial polydactyly
T7 226-246 HP:0001199 denotes triphalangeal thumbs
T8 248-264 HP:0002023 denotes imperforate anus
T9 270-289 HP:0000792 denotes renal malformations
T10 368-386 HP:0001249 denotes mental retardation
T1 59-77 HP:0000006 denotes autosomal dominant
T2 119-138 HP:0003828 denotes variable expression
T3 163-185 HP:0000356 denotes external ear anomalies
T4 187-199 HP:0000365 denotes hearing loss
T5 201-221 HP:0001841 denotes preaxial polydactyly
T6 201-221 HP:0001177 denotes preaxial polydactyly
T7 226-246 HP:0001199 denotes triphalangeal thumbs
T8 248-264 HP:0002023 denotes imperforate anus
T9 270-289 HP:0000792 denotes renal malformations
T10 368-386 HP:0001249 denotes mental retardation
T1 59-77 HP:0000006 denotes autosomal dominant
T2 119-138 HP:0003828 denotes variable expression
T3 163-185 HP:0000356 denotes external ear anomalies
T4 187-199 HP:0000365 denotes hearing loss
T5 201-221 HP:0001841 denotes preaxial polydactyly
T6 201-221 HP:0001177 denotes preaxial polydactyly
T7 226-246 HP:0001199 denotes triphalangeal thumbs
T8 248-264 HP:0002023 denotes imperforate anus
T9 270-289 HP:0000792 denotes renal malformations
T10 368-386 HP:0001249 denotes mental retardation

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 0-22 DiseaseOrPhenotypicFeature denotes Townes-Brocks syndrome 0007142
T2 24-46 DiseaseOrPhenotypicFeature denotes Townes-Brocks syndrome 0007142
T3 48-51 DiseaseOrPhenotypicFeature denotes TBS 0007142
T4 187-199 DiseaseOrPhenotypicFeature denotes hearing loss 0005365
T5 210-221 DiseaseOrPhenotypicFeature denotes polydactyly 0021003
T6 226-246 DiseaseOrPhenotypicFeature denotes triphalangeal thumbs 0008270
T7 248-264 DiseaseOrPhenotypicFeature denotes imperforate anus 0001046
T8 310-332 DiseaseOrPhenotypicFeature denotes Townes-Brocks syndrome 0007142
T9 368-386 DiseaseOrPhenotypicFeature denotes mental retardation 0001071