PubMed:16423994 / 125-408
Annnotations
c_corpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T34 | 24-41 | D015179 | denotes | colorectal cancer |
| T35 | 24-41 | D015179 | denotes | colorectal cancer |
| T36 | 151-154 | GO:0005574 | denotes | DNA |
| T38 | 151-154 | SO:0000352 | denotes | DNA |
| T37 | 151-154 | CHEBI:16991 | denotes | DNA |
| T39 | 151-154 | D004247 | denotes | DNA |
| T40 | 155-170 | GO:0006298 | denotes | mismatch repair |
| T41 | 192-196 | PR:Q9ZRV4 | denotes | MLH1 |
| T42 | 192-196 | PR:P38920 | denotes | MLH1 |
| T43 | 192-196 | PR:Q54KD8 | denotes | MLH1 |
| T45 | 192-196 | PR:Q9JK91 | denotes | MLH1 |
| T46 | 192-196 | PR:P97679 | denotes | MLH1 |
| T47 | 192-196 | PR:Q9P7W6 | denotes | MLH1 |
| T48 | 192-196 | PR:000010442 | denotes | MLH1 |
| T49 | 192-196 | PR:P40692 | denotes | MLH1 |
| T44 | 192-196 | CVCL_G669 | denotes | MLH1 |
| T51 | 201-204 | CHEBI:16768 | denotes | MSH |
| T55 | 201-204 | D009074 | denotes | MSH |
| T56 | 201-204 | D009074 | denotes | MSH |
| T57 | 201-205 | PR:000010666 | denotes | MSH2 |
| T58 | 201-205 | PR:P25847 | denotes | MSH2 |
| T59 | 201-205 | PR:P43246 | denotes | MSH2 |
| T60 | 201-205 | P22711 | denotes | MSH2 |
| T61 | 201-205 | PR:P22711 | denotes | MSH2 |
| T62 | 201-205 | PR:P54275 | denotes | MSH2 |
| T63 | 201-205 | PR:O74773 | denotes | MSH2 |
| T64 | 201-205 | PR:P43247 | denotes | MSH2 |
| T65 | 201-205 | PR:Q553L4 | denotes | MSH2 |
| T66 | 201-205 | PR:O24617 | denotes | MSH2 |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 35-41 | HP_0002664 | denotes | cancer |
| T2 | 56-76 | HP_0000006 | denotes | autosomal dominantly |
| T3 | 56-86 | HP_0000006 | denotes | autosomal dominantly inherited |
| T4 | 87-93 | HP_0002664 | denotes | cancer |
UseCases_ArguminSci_Discourse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-283 | DRI_Background | denotes | Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, predominantly MLH1 and MSH2, with large genomic rearrangements accounting for 5% to 20% of all mutations. |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 201-205 | gene:4436 | denotes | MSH2 |
| T3 | 0-41 | disease:C1333990 | denotes | Hereditary nonpolyposis colorectal cancer |
| T4 | 192-196 | gene:4292 | denotes | MLH1 |
| T5 | 0-41 | disease:C1333990 | denotes | Hereditary nonpolyposis colorectal cancer |
| R2 | T2 | T3 | associated_with | MSH2,Hereditary nonpolyposis colorectal cancer |
| R3 | T4 | T5 | associated_with | MLH1,Hereditary nonpolyposis colorectal cancer |