Source:http://linkedlifedata.com/resource/lhgdn/association:54331
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
suggest a model of how DNA is bound to the XPD protein, and can rationalize several of the mutations in the human XPD gene that lead to one of three severe diseases, xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy
|
| lhgdn:mesh_code |
D003057
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |