PubMed:9391889
Annnotations
NCBI-Disease-Corpus-GPT5-withguidelines
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 321-339 | SpecificDisease | denotes | childhood onset DM |
| T5 | 367-383 | SpecificDisease | denotes | adult type of DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 607-621 | SpecificDisease | denotes | adult onset DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-GPT5-noguidelines
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | CompositeMention | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | CompositeMention | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 321-339 | CompositeMention | denotes | childhood onset DM |
| T5 | 367-383 | CompositeMention | denotes | adult type of DM |
| T6 | 462-475 | CompositeMention | denotes | congenital DM |
| T7 | 558-571 | CompositeMention | denotes | congenital DM |
| T8 | 607-621 | CompositeMention | denotes | adult onset DM |
| T9 | 746-759 | CompositeMention | denotes | congenital DM |
| T10 | 946-959 | CompositeMention | denotes | congenital DM |
| T11 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-GPT5-guidelineprompt
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 321-339 | SpecificDisease | denotes | childhood onset DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 607-621 | SpecificDisease | denotes | adult onset DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-Moderated1
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 321-339 | SpecificDisease | denotes | childhood onset DM |
| T5 | 367-383 | SpecificDisease | denotes | adult type of DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 607-621 | SpecificDisease | denotes | adult onset DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 265-285 | HP:0011968 | denotes | feeding difficulties |
| AB2 | 573-592 | HP:0000144 | denotes | Decreased fertility |
NCBIDiseaseCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease:D009223 | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease:D009223 | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease:D009223 | denotes | DM |
| T4 | 170-187 | Modifier:D008607 | denotes | mentally retarded |
| T5 | 212-229 | DiseaseClass:D018908 | denotes | muscular weakness |
| T6 | 337-339 | SpecificDisease:D009223 | denotes | DM |
| T7 | 381-383 | SpecificDisease:D009223 | denotes | DM |
| T8 | 462-475 | SpecificDisease:D009223 | denotes | congenital DM |
| T9 | 558-571 | SpecificDisease:D009223 | denotes | congenital DM |
| T10 | 619-621 | SpecificDisease:D009223 | denotes | DM |
| T11 | 746-759 | SpecificDisease:D009223 | denotes | congenital DM |
| T12 | 946-959 | SpecificDisease:D009223 | denotes | congenital DM |
| T13 | 1003-1016 | SpecificDisease:D009223 | denotes | congenital DM |
| T14 | 1065-1067 | SpecificDisease:D009223 | denotes | DM |
NCBI-Disease-Test
| Id | Subject | Object | Predicate | Lexical cue | database_id |
|---|---|---|---|---|---|
| T927 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy | D009223 |
| T928 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy | D009223 |
| T929 | 135-137 | SpecificDisease | denotes | DM | D009223 |
| T930 | 170-187 | Modifier | denotes | mentally retarded | D008607 |
| T931 | 212-229 | DiseaseClass | denotes | muscular weakness | D018908 |
| T932 | 337-339 | SpecificDisease | denotes | DM | D009223 |
| T933 | 381-383 | SpecificDisease | denotes | DM | D009223 |
| T934 | 462-475 | SpecificDisease | denotes | congenital DM | D009223 |
| T935 | 558-571 | SpecificDisease | denotes | congenital DM | D009223 |
| T936 | 619-621 | SpecificDisease | denotes | DM | D009223 |
| T937 | 746-759 | SpecificDisease | denotes | congenital DM | D009223 |
| T938 | 946-959 | SpecificDisease | denotes | congenital DM | D009223 |
| T939 | 1003-1016 | SpecificDisease | denotes | congenital DM | D009223 |
| T940 | 1065-1067 | SpecificDisease | denotes | DM | D009223 |
NCBI-Disease-Test-Assistant-Knowledge
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 321-339 | CompositeMention | denotes | childhood onset DM |
| T4 | 367-383 | CompositeMention | denotes | adult type of DM |
| T5 | 462-475 | SpecificDisease | denotes | congenital DM |
| T6 | 558-571 | SpecificDisease | denotes | congenital DM |
| T7 | 607-621 | CompositeMention | denotes | adult onset DM |
| T8 | 746-759 | SpecificDisease | denotes | congenital DM |
| T9 | 946-959 | SpecificDisease | denotes | congenital DM |
| T10 | 1003-1016 | SpecificDisease | denotes | congenital DM |
NCBI-Disease-Test-4o-NoGuidelineInPrompt
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-138 | SpecificDisease | denotes | congenital myotonic dystrophy (DM) |
| T3 | 170-187 | Modifier | denotes | mentally retarded |
| T4 | 205-211 | Modifier | denotes | severe |
| T5 | 212-229 | CompositeMention | denotes | muscular weakness |
| T6 | 249-285 | CompositeMention | denotes | respiratory and feeding difficulties |
| T7 | 321-339 | SpecificDisease | denotes | childhood onset DM |
| T8 | 367-383 | SpecificDisease | denotes | adult type of DM |
| T9 | 462-475 | SpecificDisease | denotes | congenital DM |
| T10 | 519-530 | Modifier | denotes | sex related |
| T11 | 558-571 | SpecificDisease | denotes | congenital DM |
| T12 | 573-582 | Modifier | denotes | Decreased |
| T13 | 607-621 | SpecificDisease | denotes | adult onset DM |
| T14 | 693-706 | Modifier | denotes | almost absent |
| T15 | 746-759 | SpecificDisease | denotes | congenital DM |
| T16 | 845-852 | Modifier | denotes | shorter |
| T17 | 882-893 | Modifier | denotes | less severe |
| T18 | 946-959 | SpecificDisease | denotes | congenital DM |
| T19 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T20 | 1020-1024 | Modifier | denotes | rare |
| T21 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-o3-2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 321-339 | SpecificDisease | denotes | childhood onset DM |
| T5 | 367-383 | SpecificDisease | denotes | adult type of DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 607-621 | SpecificDisease | denotes | adult onset DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-high-o3-1
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-high-o3-2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 321-339 | SpecificDisease | denotes | childhood onset DM |
| T5 | 367-383 | SpecificDisease | denotes | adult type of DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 607-621 | SpecificDisease | denotes | adult onset DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Test-4o-GuidelineInPrompt
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 337-339 | SpecificDisease | denotes | DM |
| T4 | 381-383 | SpecificDisease | denotes | DM |
| T5 | 462-475 | SpecificDisease | denotes | congenital DM |
| T6 | 558-571 | SpecificDisease | denotes | congenital DM |
| T7 | 619-621 | SpecificDisease | denotes | DM |
| T8 | 746-759 | SpecificDisease | denotes | congenital DM |
| T9 | 946-959 | SpecificDisease | denotes | congenital DM |
| T10 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T11 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-UpdatedGuideline
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-humanintheloop
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-rezarta1
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 473-475 | SpecificDisease | denotes | DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-All
| Id | Subject | Object | Predicate | Lexical cue | database_id |
|---|---|---|---|---|---|
| T927 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy | D009223 |
| T928 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy | D009223 |
| T929 | 135-137 | SpecificDisease | denotes | DM | D009223 |
| T930 | 170-187 | Modifier | denotes | mentally retarded | D008607 |
| T931 | 212-229 | DiseaseClass | denotes | muscular weakness | D018908 |
| T932 | 337-339 | SpecificDisease | denotes | DM | D009223 |
| T933 | 381-383 | SpecificDisease | denotes | DM | D009223 |
| T934 | 462-475 | SpecificDisease | denotes | congenital DM | D009223 |
| T935 | 558-571 | SpecificDisease | denotes | congenital DM | D009223 |
| T936 | 619-621 | SpecificDisease | denotes | DM | D009223 |
| T937 | 746-759 | SpecificDisease | denotes | congenital DM | D009223 |
| T938 | 946-959 | SpecificDisease | denotes | congenital DM | D009223 |
| T939 | 1003-1016 | SpecificDisease | denotes | congenital DM | D009223 |
| T940 | 1065-1067 | SpecificDisease | denotes | DM | D009223 |
NCBI-Disease-Corpus-2stage-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 473-475 | SpecificDisease | denotes | DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-rezarta-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-4oGuideline-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 337-339 | SpecificDisease | denotes | DM |
| T4 | 381-383 | SpecificDisease | denotes | DM |
| T5 | 473-475 | SpecificDisease | denotes | DM |
| T6 | 569-571 | SpecificDisease | denotes | DM |
| T7 | 619-621 | SpecificDisease | denotes | DM |
| T8 | 757-759 | SpecificDisease | denotes | DM |
| T9 | 957-959 | SpecificDisease | denotes | DM |
| T10 | 1014-1016 | SpecificDisease | denotes | DM |
| T11 | 1065-1067 | SpecificDisease | denotes | DM |
NCBI-Disease-Corpus-Simple-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
123456
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |
12345
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 25-54 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T2 | 104-133 | SpecificDisease | denotes | congenital myotonic dystrophy |
| T3 | 135-137 | SpecificDisease | denotes | DM |
| T4 | 337-339 | SpecificDisease | denotes | DM |
| T5 | 381-383 | SpecificDisease | denotes | DM |
| T6 | 462-475 | SpecificDisease | denotes | congenital DM |
| T7 | 558-571 | SpecificDisease | denotes | congenital DM |
| T8 | 619-621 | SpecificDisease | denotes | DM |
| T9 | 746-759 | SpecificDisease | denotes | congenital DM |
| T10 | 946-959 | SpecificDisease | denotes | congenital DM |
| T11 | 1003-1016 | SpecificDisease | denotes | congenital DM |
| T12 | 1065-1067 | SpecificDisease | denotes | DM |