PubMed:10581038 / 110-325
Annnotations
c_corpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T34 | 11-18 | D004194 | denotes | disease |
| T35 | 11-18 | D004194 | denotes | disease |
| T36 | 28-46 | C566739 | denotes | autosomal dominant |
| T39 | 60-86 | D019636 | denotes | neurodegenerative disorder |
| T40 | 60-86 | D019636 | denotes | neurodegenerative disorder |
| T41 | 113-116 | CVCL_D569 | denotes | CAG |
| T42 | 117-123 | SO:0001068 | denotes | repeat |
| T43 | 124-132 | SO:0000001 | denotes | sequence |
| T48 | 173-182 | 4885 | denotes | glutamine |
| T44 | 173-182 | SO:0001448 | denotes | glutamine |
| T45 | 173-182 | D005973 | denotes | glutamine |
| T46 | 173-182 | CHEBI:28300 | denotes | glutamine |
| T47 | 173-182 | CHEBI:18050 | denotes | glutamine |
| T49 | 173-182 | D005973 | denotes | glutamine |
| T54 | 207-214 | SO:0000104 | denotes | protein |
| T53 | 207-214 | PR:000000001 | denotes | protein |
| T50 | 207-214 | GO:0003675 | denotes | protein |
| T51 | 207-214 | CHEBI:36080 | denotes | protein |
| T52 | 207-214 | CHEBI:11122 | denotes | protein |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 28-46 | HP_0000006 | denotes | autosomal dominant |
UseCases_ArguminSci_Discourse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-215 | DRI_Background | denotes | Huntington disease (HD), an autosomal dominant, progressive neurodegenerative disorder, is caused by an expanded CAG repeat sequence leading to an increase in the number of glutamine residues in the encoded protein. |