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PubMed:10602116 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 125-162 HP_0008527 denotes congenital sensorineural hearing loss
T2 136-162 HP_0000407 denotes sensorineural hearing loss
T3 150-162 HP_0000365 denotes hearing loss
T4 172-178 HP_0000853 denotes goiter
T5 236-255 HP_0000007 denotes autosomal recessive
T6 537-556 HP_0000365 denotes congenital deafness
T7 548-556 HP_0000365 denotes deafness
T8 780-786 HP_0000853 denotes goiter
T9 1148-1171 HP_0000365 denotes congenital hearing loss
T10 1159-1171 HP_0000365 denotes hearing loss
T11 1188-1219 HP_0011390 denotes inner ear morphological anomaly
T12 1253-1259 HP_0000853 denotes goiter

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10602116-0#75#78#gene5172 75-78 gene5172 denotes PDS
10602116-0#0#16#diseaseC0271829 0-16 diseaseC0271829 denotes Pendred syndrome
75#78#gene51720#16#diseaseC0271829 10602116-0#75#78#gene5172 10602116-0#0#16#diseaseC0271829 associated_with PDS,Pendred syndrome

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 0-16 SpecificDisease:C536648 denotes Pendred syndrome
T2 75-78 Modifier:C536648 denotes PDS
T3 98-114 SpecificDisease:C536648 denotes Pendred syndrome
T4 125-162 SpecificDisease:D006319 denotes congenital sensorineural hearing loss
T5 164-178 SpecificDisease:D006042 denotes thyroid goiter
T6 236-264 DiseaseClass:D030342 denotes autosomal recessive disorder
T7 308-311 Modifier:C536648 denotes PDS
T8 395-398 Modifier:C536648 denotes PDS
T9 537-556 SpecificDisease:D003638 denotes congenital deafness
T10 639-666 SpecificDisease:OMIM:600791 denotes widened vestibular aqueduct
T11 780-786 SpecificDisease:D006042 denotes goiter
T12 1014-1030 SpecificDisease:C536648 denotes Pendred syndrome
T13 1082-1085 Modifier:C536648 denotes PDS
T14 1148-1171 SpecificDisease:D003638 denotes congenital hearing loss
T15 1188-1219 SpecificDisease:D007759 denotes inner ear morphological anomaly
T16 1245-1259 SpecificDisease:D006042 denotes thyroid goiter

DisGeNET

Id Subject Object Predicate Lexical cue
T0 395-398 gene:5172 denotes PDS
T1 537-556 disease:C0339789 denotes congenital deafness
T2 1082-1085 gene:5172 denotes PDS
T3 1148-1171 disease:C0262435 denotes congenital hearing loss
T4 1082-1085 gene:5730 denotes PDS
T5 1014-1030 disease:C0271829 denotes Pendred syndrome
T6 1082-1085 gene:5172 denotes PDS
T7 1014-1030 disease:C0271829 denotes Pendred syndrome
T8 1082-1085 gene:5730 denotes PDS
T9 1148-1171 disease:C0262435 denotes congenital hearing loss
T10 1082-1085 gene:5172 denotes PDS
T11 1245-1259 disease:C0018021 denotes thyroid goiter
T12 1082-1085 gene:5730 denotes PDS
T13 1245-1259 disease:C0018021 denotes thyroid goiter
R1 T0 T1 associated_with PDS,congenital deafness
R2 T2 T3 associated_with PDS,congenital hearing loss
R3 T4 T5 associated_with PDS,Pendred syndrome
R4 T6 T7 associated_with PDS,Pendred syndrome
R5 T8 T9 associated_with PDS,congenital hearing loss
R6 T10 T11 associated_with PDS,thyroid goiter
R7 T12 T13 associated_with PDS,thyroid goiter

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T854 0-16 SpecificDisease denotes Pendred syndrome C536648
T855 75-78 Modifier denotes PDS C536648
T856 98-114 SpecificDisease denotes Pendred syndrome C536648
T857 125-162 SpecificDisease denotes congenital sensorineural hearing loss D006319
T858 164-178 SpecificDisease denotes thyroid goiter D006042
T859 236-264 DiseaseClass denotes autosomal recessive disorder D030342
T860 308-311 Modifier denotes PDS C536648
T861 395-398 Modifier denotes PDS C536648
T862 537-556 SpecificDisease denotes congenital deafness D003638
T863 639-666 SpecificDisease denotes widened vestibular aqueduct OMIM:600791
T864 780-786 SpecificDisease denotes goiter D006042
T865 1014-1030 SpecificDisease denotes Pendred syndrome C536648
T866 1082-1085 Modifier denotes PDS C536648
T867 1148-1171 SpecificDisease denotes congenital hearing loss D003638
T868 1188-1219 SpecificDisease denotes inner ear morphological anomaly D007759
T869 1245-1259 SpecificDisease denotes thyroid goiter D006042

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T854 0-16 SpecificDisease denotes Pendred syndrome C536648
T855 75-78 Modifier denotes PDS C536648
T856 98-114 SpecificDisease denotes Pendred syndrome C536648
T857 125-162 SpecificDisease denotes congenital sensorineural hearing loss D006319
T858 164-178 SpecificDisease denotes thyroid goiter D006042
T859 236-264 DiseaseClass denotes autosomal recessive disorder D030342
T860 308-311 Modifier denotes PDS C536648
T861 395-398 Modifier denotes PDS C536648
T862 537-556 SpecificDisease denotes congenital deafness D003638
T863 639-666 SpecificDisease denotes widened vestibular aqueduct OMIM:600791
T864 780-786 SpecificDisease denotes goiter D006042
T865 1014-1030 SpecificDisease denotes Pendred syndrome C536648
T866 1082-1085 Modifier denotes PDS C536648
T867 1148-1171 SpecificDisease denotes congenital hearing loss D003638
T868 1188-1219 SpecificDisease denotes inner ear morphological anomaly D007759
T869 1245-1259 SpecificDisease denotes thyroid goiter D006042

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 98-114 SpecificDisease denotes Pendred syndrome
T2 125-162 SpecificDisease denotes congenital sensorineural hearing loss
T3 164-178 SpecificDisease denotes thyroid goiter
T4 236-264 DiseaseClass denotes autosomal recessive disorder
T5 537-556 SpecificDisease denotes congenital deafness
T6 780-786 SpecificDisease denotes goiter
T7 1014-1030 SpecificDisease denotes Pendred syndrome
T8 1148-1171 SpecificDisease denotes congenital hearing loss
T9 1245-1259 SpecificDisease denotes thyroid goiter

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 98-114 SpecificDisease denotes Pendred syndrome
T2 125-162 DiseaseClass denotes congenital sensorineural hearing loss
T3 164-178 SpecificDisease denotes thyroid goiter
T4 528-556 DiseaseClass denotes profound congenital deafness
T5 780-786 SpecificDisease denotes goiter
T6 1014-1030 SpecificDisease denotes Pendred syndrome
T7 1139-1171 DiseaseClass denotes profound congenital hearing loss
T8 1245-1259 SpecificDisease denotes thyroid goiter

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 0-16 SpecificDisease denotes Pendred syndrome
T2 98-114 SpecificDisease denotes Pendred syndrome
T3 125-162 Modifier denotes congenital sensorineural hearing loss
T4 164-178 Modifier denotes thyroid goiter
T5 236-264 DiseaseClass denotes autosomal recessive disorder
T6 528-556 Modifier denotes profound congenital deafness
T7 780-786 Modifier denotes goiter
T8 1014-1030 SpecificDisease denotes Pendred syndrome
T9 1129-1171 Modifier denotes severe to profound congenital hearing loss
T10 1245-1259 Modifier denotes thyroid goiter

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-16 SpecificDisease denotes Pendred syndrome
T2 98-114 SpecificDisease denotes Pendred syndrome
T3 125-135 Modifier denotes congenital
T4 136-162 SpecificDisease denotes sensorineural hearing loss
T5 164-178 SpecificDisease denotes thyroid goiter
T6 236-255 Modifier denotes autosomal recessive
T7 256-264 SpecificDisease denotes disorder
T8 528-547 Modifier denotes profound congenital
T9 548-556 SpecificDisease denotes deafness
T10 780-786 SpecificDisease denotes goiter
T11 1014-1030 SpecificDisease denotes Pendred syndrome
T12 1129-1158 Modifier denotes severe to profound congenital
T13 1159-1171 SpecificDisease denotes hearing loss
T14 1188-1197 Modifier denotes inner ear
T15 1245-1259 SpecificDisease denotes thyroid goiter