PubMed:24942733 / 163-338
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-175 | Sentence | denotes | Mutations in the gene encoding leucine-rich repeat kinase 2 (LRRK2) are a common genetic cause of Parkinson disease, but the mechanisms whereby LRRK2 is regulated are unknown. |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 98-107 | HP_0001300 | denotes | Parkinson |
Allie
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| SS1_24942733_1_0 | 31-59 | expanded | denotes | leucine-rich repeat kinase 2 |
| SS2_24942733_1_0 | 61-66 | abbr | denotes | LRRK2 |
| AE1_24942733_1_0 | SS1_24942733_1_0 | SS2_24942733_1_0 | abbreviatedTo | leucine-rich repeat kinase 2,LRRK2 |
PubMed_ArguminSci
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-175 | DRI_Approach | denotes | Mutations in the gene encoding leucine-rich repeat kinase 2 (LRRK2) are a common genetic cause of Parkinson disease, but the mechanisms whereby LRRK2 is regulated are unknown. |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 98-115 | Disease | denotes | Parkinson disease | http://purl.obolibrary.org/obo/MONDO_0005180 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 98-107 | Phenotype | denotes | Parkinson | HP:0001300 |