PubMed:16423994 / 927-1213
Annnotations
c_corpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T130 | 103-107 | PR:Q9ZRV4 | denotes | MLH1 |
| T131 | 103-107 | PR:P38920 | denotes | MLH1 |
| T132 | 103-107 | PR:Q54KD8 | denotes | MLH1 |
| T134 | 103-107 | PR:Q9JK91 | denotes | MLH1 |
| T135 | 103-107 | PR:P97679 | denotes | MLH1 |
| T136 | 103-107 | PR:Q9P7W6 | denotes | MLH1 |
| T137 | 103-107 | PR:000010442 | denotes | MLH1 |
| T138 | 103-107 | PR:P40692 | denotes | MLH1 |
| T133 | 103-107 | CVCL_G669 | denotes | MLH1 |
| T140 | 108-111 | CHEBI:16768 | denotes | MSH |
| T144 | 108-111 | D009074 | denotes | MSH |
| T145 | 108-111 | D009074 | denotes | MSH |
| T146 | 108-112 | PR:000010666 | denotes | MSH2 |
| T147 | 108-112 | PR:P25847 | denotes | MSH2 |
| T148 | 108-112 | PR:P43246 | denotes | MSH2 |
| T149 | 108-112 | P22711 | denotes | MSH2 |
| T150 | 108-112 | PR:P22711 | denotes | MSH2 |
| T151 | 108-112 | PR:P54275 | denotes | MSH2 |
| T152 | 108-112 | PR:O74773 | denotes | MSH2 |
| T153 | 108-112 | PR:P43247 | denotes | MSH2 |
| T154 | 108-112 | PR:Q553L4 | denotes | MSH2 |
| T155 | 108-112 | PR:O24617 | denotes | MSH2 |
| T156 | 113-121 | SO:0000109 | denotes | mutation |
| T157 | 122-130 | CHEBI:78059 | denotes | carriers |
| T158 | 182-204 | SO:0001786 | denotes | loss of heterozygosity |
| T159 | 236-242 | D009369 | denotes | tumors |
| T160 | 236-242 | D009369 | denotes | tumors |
| T161 | 248-252 | PR:Q9ZRV4 | denotes | MLH1 |
| T162 | 248-252 | PR:P38920 | denotes | MLH1 |
| T163 | 248-252 | PR:Q54KD8 | denotes | MLH1 |
| T165 | 248-252 | PR:Q9JK91 | denotes | MLH1 |
| T166 | 248-252 | PR:P97679 | denotes | MLH1 |
| T167 | 248-252 | PR:Q9P7W6 | denotes | MLH1 |
| T168 | 248-252 | PR:000010442 | denotes | MLH1 |
| T169 | 248-252 | PR:P40692 | denotes | MLH1 |
| T164 | 248-252 | CVCL_G669 | denotes | MLH1 |
| T171 | 253-256 | CHEBI:16768 | denotes | MSH |
| T175 | 253-256 | D009074 | denotes | MSH |
| T176 | 253-256 | D009074 | denotes | MSH |
| T177 | 253-257 | PR:000010666 | denotes | MSH2 |
| T178 | 253-257 | PR:P25847 | denotes | MSH2 |
| T179 | 253-257 | PR:P43246 | denotes | MSH2 |
| T180 | 253-257 | P22711 | denotes | MSH2 |
| T181 | 253-257 | PR:P22711 | denotes | MSH2 |
| T182 | 253-257 | PR:P54275 | denotes | MSH2 |
| T183 | 253-257 | PR:O74773 | denotes | MSH2 |
| T184 | 253-257 | PR:P43247 | denotes | MSH2 |
| T185 | 253-257 | PR:Q553L4 | denotes | MSH2 |
| T186 | 253-257 | PR:O24617 | denotes | MSH2 |
| T187 | 268-276 | SO:0000159 | denotes | deletion |
| T188 | 277-285 | CHEBI:78059 | denotes | carriers |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T7 | 236-242 | HP_0002664 | denotes | tumors |
UseCases_ArguminSci_Discourse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T5 | 0-286 | DRI_Background | denotes | The aims of the study were (a) to determine the proportion of large genomic rearrangements among Swiss MLH1/MSH2 mutation carriers and (b) to investigate the frequency and nature of loss of heterozygosity as a second, somatic event, in tumors from MLH1/MSH2 germ line deletion carriers. |