Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
gptkb:adrenal_hypoplasia_congenita
gptkb:glycerol_kinase_deficiency gptkb:Becker_muscular_dystrophy gptkb:Duchenne_muscular_dystrophy retinitis pigmentosa |
| gptkbp:deletionSyndrome |
Xp21 contiguous gene syndrome
|
| https://www.w3.org/2000/01/rdf-schema#label |
Xp21 gene
|
| gptkbp:locatedOn |
gptkb:X_chromosome
|
| gptkbp:locatedOnChromosome |
Xp21
|
| gptkbp:species |
gptkb:Homo_sapiens
|
| gptkbp:bfsParent |
gptkb:DMD_gene
|
| gptkbp:bfsLayer |
7
|