| Subject | Predicate | Object | Context |
|---|---|---|---|
| gene-rif:493937 | rdf:type | entrezgene:GeneRif | lld:entrezgene |
| gene-rif:493937 | entrezgene:geneRifText | The study reveals the high frequency of SPG11 mutations in patients with HSP, a TCC and cognitive impairment, including in isolated patients, and extends the associated phenotype. | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:geneRif | gene-rif:493937 | lld:entrezgene |