| Subject | Predicate | Object | Context |
|---|---|---|---|
| gene-rif:440019 | rdf:type | entrezgene:GeneRif | lld:entrezgene |
| gene-rif:440019 | entrezgene:geneRifText | Cognitive impairment may be another feature of the MFN2-related phenotype. The widespread peripheral and CNS involvement, as well as the neurosensorial defects, underline the similarities among MFN2-related and primary mitochondrial disorders. | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:geneRif | gene-rif:440019 | lld:entrezgene |