PubMed:2793865 / 1316-1580
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T8 | 0-264 | Sentence | denotes | The results indicate that the mutant OAT precursor from the gyrate atrophy patient can be transported to the mitochondria but is minimally processed there, which would lead to degradation of the labile precursor and loss of OAT activity as phenotypically observed. |
| T8 | 0-264 | Sentence | denotes | The results indicate that the mutant OAT precursor from the gyrate atrophy patient can be transported to the mitochondria but is minimally processed there, which would lead to degradation of the labile precursor and loss of OAT activity as phenotypically observed. |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 37-40 | gene:4942 | denotes | OAT |
| T3 | 60-74 | disease:C0018425 | denotes | gyrate atrophy |
| T4 | 224-227 | gene:4942 | denotes | OAT |
| T5 | 60-74 | disease:C0018425 | denotes | gyrate atrophy |
| R2 | T2 | T3 | associated_with | OAT,gyrate atrophy |
| R3 | T4 | T5 | associated_with | OAT,gyrate atrophy |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T20 | 37-40 | Disease | denotes | OAT | http://purl.obolibrary.org/obo/MONDO_0004483 |
| T21 | 60-74 | Disease | denotes | gyrate atrophy | http://purl.obolibrary.org/obo/MONDO_0009796 |
| T22 | 224-227 | Disease | denotes | OAT | http://purl.obolibrary.org/obo/MONDO_0004483 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T3 | 75-82 | OrganismTaxon | denotes | patient | 9606 |