PubMed:2793865 / 107-338
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-231 | Sentence | denotes | A generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy, an autosomal recessive degenerative disease of the choroid and retina of the eye that leads to blindness. |
| T2 | 0-231 | Sentence | denotes | A generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy, an autosomal recessive degenerative disease of the choroid and retina of the eye that leads to blindness. |
Glycosmos6-MAT
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 189-195 | http://purl.obolibrary.org/obo/MAT_0000142 | denotes | retina |
| T2 | 203-206 | http://purl.obolibrary.org/obo/MAT_0000140 | denotes | eye |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 32-45 | HP_0001427 | denotes | mitochondrial |
| T2 | 129-148 | HP_0000007 | denotes | autosomal recessive |
| T3 | 221-230 | HP_0000618 | denotes | blindness |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 2793865-1#82#85#gene4942 | 82-85 | gene4942 | denotes | OAT |
| 2793865-1#149#169#diseaseC1285162 | 149-169 | diseaseC1285162 | denotes | degenerative disease |
| 82#85#gene4942149#169#diseaseC1285162 | 2793865-1#82#85#gene4942 | 2793865-1#149#169#diseaseC1285162 | associated_with | OAT,degenerative disease |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 221-230 | HP:0000618 | denotes | blindness |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 82-85 | Disease | denotes | OAT | http://purl.obolibrary.org/obo/MONDO_0004483 |
| T3 | 110-124 | Disease | denotes | gyrate atrophy | http://purl.obolibrary.org/obo/MONDO_0009796 |
| T4 | 149-169 | Disease | denotes | degenerative disease | http://purl.obolibrary.org/obo/MONDO_0005559|http://purl.obolibrary.org/obo/MONDO_0024236 |
| T6 | 221-230 | Disease | denotes | blindness | http://purl.obolibrary.org/obo/MONDO_0001941 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 221-230 | Phenotype | denotes | blindness | HP:0000618 |
Anatomy-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 177-195 | Body_part | denotes | choroid and retina | http://purl.obolibrary.org/obo/UBERON_0019207 |
| T2 | 203-206 | Body_part | denotes | eye | http://purl.obolibrary.org/obo/UBERON_0000019|http://purl.obolibrary.org/obo/UBERON_0000970|http://purl.obolibrary.org/obo/UBERON_0010230 |
Anatomy-MAT
| Id | Subject | Object | Predicate | Lexical cue | mat_id |
|---|---|---|---|---|---|
| T1 | 189-195 | Body_part | denotes | retina | http://purl.obolibrary.org/obo/MAT_0000142 |
| T2 | 203-206 | Body_part | denotes | eye | http://purl.obolibrary.org/obo/MAT_0000140 |