PubMed:7191069 / 192-218
Annnotations
NCBIDiseaseCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T7 | 13-26 | SpecificDisease:OMIM:217000 | denotes | C2 deficiency |
NCBI-Disease-Train
| Id | Subject | Object | Predicate | Lexical cue | database_id |
|---|---|---|---|---|---|
| T4368 | 13-26 | SpecificDisease | denotes | C2 deficiency | OMIM:217000 |
NCBI-Disease-Corpus-All
| Id | Subject | Object | Predicate | Lexical cue | database_id |
|---|---|---|---|---|---|
| T4368 | 13-26 | SpecificDisease | denotes | C2 deficiency | OMIM:217000 |
NCBI-Disease-Corpus-rezarta-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T6 | 13-26 | SpecificDisease | denotes | C2 deficiency |
NCBI-Disease-Corpus-4oGuideline-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T5 | 0-26 | SpecificDisease | denotes | heterozygous C2 deficiency |
NCBI-Disease-Corpus-Simple-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T5 | 0-26 | CompositeMention | denotes | heterozygous C2 deficiency |