| Typicality: | 0.293 |
| Saliency: | 0.534 |
| for hereditary cancer | 10 | transitive-object |
| in people | 7 | other |
| for crohn’s disease in homo | 7 | transitive-object |
| mutation → be associated with → increased risk | 21 |
| mutation → be linked to → increased risk | 4 |
| mutation → lead to → increased risk | 4 |
| mutation → cause → increased risk | 4 |
| mutation → confer → greater risk | 3 |
| mutation → give → increased risk | 3 |
| mutation → be associated with → higher risk | 3 |
| negative | neutral | positive |
| 0.677 | 0.308 | 0.015 |
| Raw frequency | 42 |
| Normalized frequency | 0.534 |
| Modifier score | 0.200 |
| Perplexity | 112.503 |