Source:http://linkedlifedata.com/resource/lhgdn/association:32378
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Relationship between the molecular defect in the FMR1 gene and the clinical phenotype associated with fragile x syndrome.
|
| lhgdn:mesh_code |
D005600
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |