PubMed:17409200 / 0-258
Annnotations
c_corpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 8-14 | SO:0001068 | denotes | repeat |
| T2 | 15-23 | SO:0000109 | denotes | mutation |
| T5 | 88-106 | D006816 | denotes | Huntington disease |
| T6 | 88-106 | D006816 | denotes | Huntington disease |
| T9 | 107-112 | UBERON:6110636 | denotes | brain |
| T10 | 107-112 | UBERON:0000955 | denotes | brain |
| T11 | 125-132 | D004194 | denotes | disease |
| T12 | 125-132 | D004194 | denotes | disease |
| T13 | 165-168 | CVCL_D569 | denotes | CAG |
| T14 | 169-175 | SO:0001068 | denotes | repeat |
| T19 | 197-206 | 4885 | denotes | glutamine |
| T15 | 197-206 | SO:0001448 | denotes | glutamine |
| T16 | 197-206 | D005973 | denotes | glutamine |
| T17 | 197-206 | CHEBI:28300 | denotes | glutamine |
| T18 | 197-206 | CHEBI:18050 | denotes | glutamine |
| T20 | 197-206 | D005973 | denotes | glutamine |
| T21 | 207-212 | UBERON:0001018 | denotes | tract |
| T26 | 218-225 | SO:0000104 | denotes | protein |
| T25 | 218-225 | PR:000000001 | denotes | protein |
| T22 | 218-225 | GO:0003675 | denotes | protein |
| T23 | 218-225 | CHEBI:36080 | denotes | protein |
| T24 | 218-225 | CHEBI:11122 | denotes | protein |
| T27 | 233-243 | P42858 | denotes | huntingtin |
| T28 | 233-243 | P42859 | denotes | huntingtin |
| T29 | 233-243 | P51111 | denotes | huntingtin |
| T30 | 233-243 | PR:000008840 | denotes | huntingtin |
| T31 | 233-243 | P51112 | denotes | huntingtin |
UseCases_ArguminSci_Discourse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-113 | DRI_Outcome | denotes | Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain. |
| T2 | 114-244 | DRI_Background | denotes | Huntington disease is caused by the expansion of a CAG repeat encoding an extended glutamine tract in a protein called huntingtin. |