PubMed:11301317 / 151-328
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T3 | 0-177 | Sentence | denotes | Rieger syndrome is an autosomal-dominant human disorder characterized by glaucoma as well as dental hypoplasia, mild craniofacial dysmorphism, and umbilical stump abnormalities. |
| T3 | 0-177 | Sentence | denotes | Rieger syndrome is an autosomal-dominant human disorder characterized by glaucoma as well as dental hypoplasia, mild craniofacial dysmorphism, and umbilical stump abnormalities. |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 73-81 | HP:0000501 | denotes | glaucoma |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB2 | 0-15 | ORDO:782 | denotes | Rieger syndrome |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T3 | 0-15 | Disease | denotes | Rieger syndrome | http://purl.obolibrary.org/obo/MONDO_0019187 |
| T4 | 73-81 | Disease | denotes | glaucoma | http://purl.obolibrary.org/obo/MONDO_0005041 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 73-81 | Phenotype | denotes | glaucoma | HP:0000501 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 41-46 | OrganismTaxon | denotes | human | 9606 |
| T2 | 73-81 | OrganismTaxon | denotes | glaucoma | 5882 |