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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
8595416-1#148#152#gene1760 282-286 gene1760 denotes DMPK
8595416-1#0#18#diseaseC0027126 134-152 diseaseC0027126 denotes Myotonic dystrophy
8595416-1#20#22#diseaseC0027126 154-156 diseaseC0027126 denotes DM
148#152#gene17600#18#diseaseC0027126 8595416-1#148#152#gene1760 8595416-1#0#18#diseaseC0027126 associated_with DMPK,Myotonic dystrophy
148#152#gene176020#22#diseaseC0027126 8595416-1#148#152#gene1760 8595416-1#20#22#diseaseC0027126 associated_with DMPK,DM

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier:D009223 denotes myotonic dystrophy
T2 134-152 SpecificDisease:D009223 denotes Myotonic dystrophy
T3 154-156 SpecificDisease:D009223 denotes DM
T4 560-562 Modifier:D009223 denotes DM
T5 1232-1234 Modifier:D009223 denotes DM

ncbi-valid

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 Modifier denotes DM
T5 1232-1234 Modifier denotes DM

ncbi-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 SpecificDisease denotes DM

ncbi-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 Modifier denotes DM
T5 1232-1234 Modifier denotes DM

ncbi-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 SpecificDisease denotes DM
T5 1232-1234 SpecificDisease denotes DM

ncbi-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 Modifier denotes DM
T5 1232-1234 Modifier denotes DM

ncbi-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 474-476 SpecificDisease denotes DM
T5 750-770 SpecificDisease denotes chromatin disruption

ncbi-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 474-476 Modifier denotes DM
T5 845-847 Modifier denotes DM

ncbi-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM

ncbi-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-7 Modifier denotes A novel
T2 8-28 CompositeMention denotes homeodomain-encoding
T3 29-33 CompositeMention denotes gene
T4 91-109 SpecificDisease denotes myotonic dystrophy
T5 110-118 Modifier denotes unstable
T6 119-125 CompositeMention denotes (CTG)n
T7 126-132 CompositeMention denotes repeat
T8 134-152 SpecificDisease denotes Myotonic dystrophy
T9 154-156 SpecificDisease denotes DM
T10 179-185 CompositeMention denotes (CTG)n
T11 186-206 CompositeMention denotes trinucleotide repeat
T12 207-216 CompositeMention denotes expansion
T13 252-259 CompositeMention denotes protein
T14 276-280 CompositeMention denotes gene
T15 282-286 CompositeMention denotes DMPK
T16 302-312 CompositeMention denotes chromosome
T17 313-318 CompositeMention denotes 19q13
T18 318-320 CompositeMention denotes .3
T19 322-338 CompositeMention denotes Characterisation
T20 474-476 SpecificDisease denotes DM
T21 479-483 CompositeMention denotes mRNA
T22 502-506 CompositeMention denotes DMPK
T23 590-599 Modifier denotes gene rich
T24 629-645 CompositeMention denotes repeat expansion
T25 685-698 CompositeMention denotes transcription
T26 699-704 CompositeMention denotes units
T27 750-759 CompositeMention denotes chromatin
T28 760-770 CompositeMention denotes disruption
T29 780-788 CompositeMention denotes searched
T30 793-798 CompositeMention denotes genes
T31 799-809 CompositeMention denotes associated
T32 817-827 CompositeMention denotes CpG island
T33 835-841 CompositeMention denotes 3' end
T34 851-861 CompositeMention denotes Sequencing
T35 912-915 CompositeMention denotes 3.5
T36 916-918 CompositeMention denotes kb
T37 945-951 CompositeMention denotes (CTG)n
T38 960-970 CompositeMention denotes Comparison
T39 974-981 CompositeMention denotes genomic
T40 982-991 CompositeMention denotes sequences
T41 992-1002 CompositeMention denotes downstream
T42 1004-1015 CompositeMention denotes centromeric
T43 1034-1039 CompositeMention denotes human
T44 1044-1049 CompositeMention denotes mouse
T45 1084-1092 CompositeMention denotes homology
T46 1100-1110 CompositeMention denotes correspond
T47 1114-1119 CompositeMention denotes exons
T48 1125-1129 CompositeMention denotes gene
T49 1152-1163 CompositeMention denotes homeodomain
T50 1164-1171 CompositeMention denotes protein
T51 1173-1179 CompositeMention denotes RT-PCR
T52 1180-1188 CompositeMention denotes analysis
T53 1232-1240 CompositeMention denotes DM locus
T54 1273-1278 CompositeMention denotes DMAHP
T55 1284-1293 CompositeMention denotes expressed
T56 1315-1322 CompositeMention denotes tissues
T57 1334-1349 CompositeMention denotes skeletal muscle
T58 1351-1356 CompositeMention denotes heart
T59 1361-1366 CompositeMention denotes brain

ncbi-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 154-156 SpecificDisease denotes DM

ncbi-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 110-118 Modifier denotes unstable
T3 134-152 SpecificDisease denotes Myotonic dystrophy
T4 154-156 SpecificDisease denotes DM

ncbi-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 282-284 Modifier denotes DM
T5 474-476 Modifier denotes DM

ncbi-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 474-476 SpecificDisease denotes DM

ncbi-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 474-476 Modifier denotes DM
T5 845-847 Modifier denotes DM

ncbi-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 91-109 Modifier denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 Modifier denotes DM
T5 1232-1234 Modifier denotes DM

ncbi-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 282-284 Modifier denotes DM
T5 560-562 Modifier denotes DM

NCBI-Disease-Develop

Id Subject Object Predicate Lexical cue database_id
T412 91-109 Modifier denotes myotonic dystrophy D009223
T413 134-152 SpecificDisease denotes Myotonic dystrophy D009223
T414 154-156 SpecificDisease denotes DM D009223
T415 560-562 Modifier denotes DM D009223
T416 1232-1234 Modifier denotes DM D009223

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T412 91-109 Modifier denotes myotonic dystrophy D009223
T413 134-152 SpecificDisease denotes Myotonic dystrophy D009223
T414 154-156 SpecificDisease denotes DM D009223
T415 560-562 Modifier denotes DM D009223
T416 1232-1234 Modifier denotes DM D009223

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 Modifier denotes DM
T5 1232-1234 Modifier denotes DM

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM
T4 560-562 Modifier denotes DM

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-152 SpecificDisease denotes Myotonic dystrophy
T3 154-156 SpecificDisease denotes DM

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 91-109 SpecificDisease denotes myotonic dystrophy
T2 134-157 SpecificDisease denotes Myotonic dystrophy (DM)