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PubMed:10767347 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 122-128 HP_0001251 denotes ataxia
T2 153-172 HP_0000007 denotes autosomal recessive
T3 173-179 HP_0001251 denotes ataxia
T4 282-295 HP_0001427 denotes mitochondrial
T5 349-362 HP_0001427 denotes mitochondrial
T6 570-583 HP_0001427 denotes mitochondrial

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10767347-1#159#167#gene2395 270-278 gene2395 denotes frataxin
10767347-1#0#17#diseaseC0016719 111-128 diseaseC0016719 denotes Friedreich ataxia
10767347-2#120#128#gene2395 501-509 gene2395 denotes frataxin
10767347-2#166#184#diseaseC0033626 547-565 diseaseC0033626 denotes protein deficiency
159#167#gene23950#17#diseaseC0016719 10767347-1#159#167#gene2395 10767347-1#0#17#diseaseC0016719 associated_with frataxin,Friedreich ataxia
120#128#gene2395166#184#diseaseC0033626 10767347-2#120#128#gene2395 10767347-2#166#184#diseaseC0033626 associated_with frataxin,protein deficiency

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 20-37 Modifier:D005621 denotes Friedreich ataxia
T2 64-83 SpecificDisease:D020964 denotes embryonic lethality
T3 111-128 SpecificDisease:D005621 denotes Friedreich ataxia
T4 130-134 SpecificDisease:D005621 denotes FRDA
T5 153-179 DiseaseClass:D013132 denotes autosomal recessive ataxia
T6 535-565 SpecificDisease:OMIM:255125 denotes iron-sulfur protein deficiency
T7 838-842 Modifier:D005621 denotes Frda
T8 897-916 SpecificDisease:D020964 denotes embryonic lethality

DisGeNET

Id Subject Object Predicate Lexical cue
T0 270-278 gene:2395 denotes frataxin
T1 111-128 disease:C0016719 denotes Friedreich ataxia
T2 501-509 gene:2395 denotes frataxin
T3 547-565 disease:C0033626 denotes protein deficiency
R1 T0 T1 associated_with frataxin,Friedreich ataxia
R2 T2 T3 associated_with frataxin,protein deficiency

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T2307 20-37 Modifier denotes Friedreich ataxia D005621
T2308 64-83 SpecificDisease denotes embryonic lethality D020964
T2309 111-128 SpecificDisease denotes Friedreich ataxia D005621
T2310 130-134 SpecificDisease denotes FRDA D005621
T2311 153-179 DiseaseClass denotes autosomal recessive ataxia D013132
T2312 535-565 SpecificDisease denotes iron-sulfur protein deficiency OMIM:255125
T2313 838-842 Modifier denotes Frda D005621
T2314 897-916 SpecificDisease denotes embryonic lethality D020964

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T2307 20-37 Modifier denotes Friedreich ataxia D005621
T2308 64-83 SpecificDisease denotes embryonic lethality D020964
T2309 111-128 SpecificDisease denotes Friedreich ataxia D005621
T2310 130-134 SpecificDisease denotes FRDA D005621
T2311 153-179 DiseaseClass denotes autosomal recessive ataxia D013132
T2312 535-565 SpecificDisease denotes iron-sulfur protein deficiency OMIM:255125
T2313 838-842 Modifier denotes Frda D005621
T2314 897-916 SpecificDisease denotes embryonic lethality D020964

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 20-37 SpecificDisease denotes Friedreich ataxia
T2 111-128 SpecificDisease denotes Friedreich ataxia
T3 130-134 SpecificDisease denotes FRDA
T4 173-179 DiseaseClass denotes ataxia

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 20-37 Modifier denotes Friedreich ataxia
T2 111-128 SpecificDisease denotes Friedreich ataxia
T3 130-134 SpecificDisease denotes FRDA
T4 838-842 Modifier denotes Frda

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 20-37 SpecificDisease denotes Friedreich ataxia
T2 111-135 SpecificDisease denotes Friedreich ataxia (FRDA)

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 20-37 SpecificDisease denotes Friedreich ataxia
T2 111-135 SpecificDisease denotes Friedreich ataxia (FRDA)
T3 173-179 DiseaseClass denotes ataxia
T4 749-756 SpecificDisease denotes disease