Statements (17)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:affects |
gptkb:skeletal_muscle
|
| gptkbp:associatedWith |
GNE gene mutation
|
| gptkbp:category |
gptkb:muscular_dystrophy
|
| gptkbp:diagnosedBy |
genetic testing
muscle biopsy |
| gptkbp:onset |
adulthood
|
| gptkbp:progression |
slow
|
| gptkbp:subspecies |
gptkb:hereditary_inclusion_body_myopathy
gptkb:sporadic_inclusion_body_myositis |
| gptkbp:symptom |
muscle weakness
progressive muscle wasting |
| gptkbp:treatment |
supportive care
physical therapy |
| gptkbp:bfsParent |
gptkb:TDP43
|
| gptkbp:bfsLayer |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
inclusion body myopathy
|