Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
|
| gptkbp:affects |
MT-TL1 gene
|
| gptkbp:associatedWith |
gptkb:mitochondrial_myopathy
gptkb:MELAS_syndrome mitochondrial diseases |
| gptkbp:cause |
gptkb:encephalopathy
lactic acidosis stroke-like episodes |
| https://www.w3.org/2000/01/rdf-schema#label |
MT-TL1 gene mutation
|
| gptkbp:location |
gptkb:mitochondrial_DNA
|
| gptkbp:mostCommonMutation |
A3243G
|
| gptkbp:bfsParent |
gptkb:MELAS_syndrome
|
| gptkbp:bfsLayer |
7
|