Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:DNA
|
| gptkbp:associated_with |
retinal diseases
|
| gptkbp:code |
elongation of very long chain fatty acids protein 4
|
| gptkbp:discovered_by |
genetic research
|
| gptkbp:function |
fatty acid elongation
|
| gptkbp:genetic_studies |
causes Stargardt disease
causes cone-rod dystrophy |
| https://www.w3.org/2000/01/rdf-schema#label |
ELOVL4
|
| gptkbp:involved_in |
fatty acid metabolism
|
| gptkbp:is_expressed_in |
retinal pigment epithelium
|
| gptkbp:located_in |
gptkb:human_chromosome_6
|
| gptkbp:bfsParent |
gptkb:Leber's_congenital_amaurosis
|
| gptkbp:bfsLayer |
6
|