Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:DNA
|
| gptkbp:associated_with |
gptkb:muscular_dystrophy
|
| gptkbp:discovered_by |
gptkb:1999
|
| gptkbp:diseases |
gptkb:muscular_dystrophy
|
| gptkbp:field_of_study |
molecular genetics
|
| gptkbp:function |
protein O-mannosyltransferase
|
| gptkbp:genetic_studies |
causes Walker-Warburg syndrome
|
| https://www.w3.org/2000/01/rdf-schema#label |
POMT1
|
| gptkbp:interacts_with |
gptkb:POMT2
|
| gptkbp:is_expressed_in |
skeletal muscle
|
| gptkbp:located_in |
human chromosome 9
|
| gptkbp:bfsParent |
gptkb:muscular_dystrophy
|
| gptkbp:bfsLayer |
5
|