PubMed:16423994 / 0-304
Annnotations
c_corpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-15 | GO:0035822 | denotes | Gene conversion |
| T2 | 63-72 | SO:0000817 | denotes | wild-type |
| T3 | 73-79 | SO:0001023 | denotes | allele |
| T4 | 83-90 | D009369 | denotes | cancers |
| T5 | 83-90 | D009369 | denotes | cancers |
| T6 | 96-100 | PR:Q9ZRV4 | denotes | MLH1 |
| T7 | 96-100 | PR:P38920 | denotes | MLH1 |
| T8 | 96-100 | PR:Q54KD8 | denotes | MLH1 |
| T10 | 96-100 | PR:Q9JK91 | denotes | MLH1 |
| T11 | 96-100 | PR:P97679 | denotes | MLH1 |
| T12 | 96-100 | PR:Q9P7W6 | denotes | MLH1 |
| T13 | 96-100 | PR:000010442 | denotes | MLH1 |
| T14 | 96-100 | PR:P40692 | denotes | MLH1 |
| T9 | 96-100 | CVCL_G669 | denotes | MLH1 |
| T16 | 101-104 | CHEBI:16768 | denotes | MSH |
| T20 | 101-104 | D009074 | denotes | MSH |
| T21 | 101-104 | D009074 | denotes | MSH |
| T22 | 101-105 | PR:000010666 | denotes | MSH2 |
| T23 | 101-105 | PR:P25847 | denotes | MSH2 |
| T24 | 101-105 | PR:P43246 | denotes | MSH2 |
| T25 | 101-105 | P22711 | denotes | MSH2 |
| T26 | 101-105 | PR:P22711 | denotes | MSH2 |
| T27 | 101-105 | PR:P54275 | denotes | MSH2 |
| T28 | 101-105 | PR:O74773 | denotes | MSH2 |
| T29 | 101-105 | PR:P43247 | denotes | MSH2 |
| T30 | 101-105 | PR:Q553L4 | denotes | MSH2 |
| T31 | 101-105 | PR:O24617 | denotes | MSH2 |
| T32 | 106-114 | SO:0000159 | denotes | deletion |
| T33 | 115-123 | CHEBI:78059 | denotes | carriers |
| T34 | 149-166 | D015179 | denotes | colorectal cancer |
| T35 | 149-166 | D015179 | denotes | colorectal cancer |
| T36 | 276-279 | GO:0005574 | denotes | DNA |
| T38 | 276-279 | SO:0000352 | denotes | DNA |
| T37 | 276-279 | CHEBI:16991 | denotes | DNA |
| T39 | 276-279 | D004247 | denotes | DNA |
| T40 | 280-295 | GO:0006298 | denotes | mismatch repair |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 160-166 | HP_0002664 | denotes | cancer |
| T2 | 181-201 | HP_0000006 | denotes | autosomal dominantly |
| T3 | 181-211 | HP_0000006 | denotes | autosomal dominantly inherited |
| T4 | 212-218 | HP_0002664 | denotes | cancer |
UseCases_ArguminSci_Discourse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-124 | DRI_Background | denotes | Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers. |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 96-100 | gene:4292 | denotes | MLH1 |
| T1 | 83-90 | disease:C0006826 | denotes | cancers |
| T3 | 125-166 | disease:C1333990 | denotes | Hereditary nonpolyposis colorectal cancer |
| T5 | 125-166 | disease:C1333990 | denotes | Hereditary nonpolyposis colorectal cancer |
| R1 | T0 | T1 | associated_with | MLH1,cancers |