PubMed:20052765 / 293-455
Annnotations
PubMed_ArguminSci
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 0-162 | DRI_Challenge | denotes | Mutations in the CLN5 gene result in the Finnish variant late infantile NCL characterized by gradual loss of vision, epileptic seizures, and mental deterioration. |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 101-115 | HP_0000572 | denotes | loss of vision |
| T2 | 127-135 | HP_0001250 | denotes | seizures |
| T3 | 141-161 | HP_0001268 | denotes | mental deterioration |