Source:http://linkedlifedata.com/resource/lhgdn/association:59802
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:59802 | lhgdn:found_in | pubmed-article:18094726 | lld:lhgdn |
| lhgdn:association:59802 | lhgdn:geneRifSource | Disruption of the gene encoding Barttin, BSND, results in a?double knockout?of the functions of both ClCKA and ClCKB, manifesting as Bartter syndrome type IV with sensorineural deafness and an especially severe salt-losing phenotype. | lld:lhgdn |
| lhgdn:association:59802 | lhgdn:mesh_code | D001477 | lld:lhgdn |
| lhgdn:association:59802 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Po... | lld:lhgdn |
| lhgdn:association:59802 | lhgdn:umls_code | umls-concept:C0004775 | lld:mappings |
| entrez-gene:1187 | lhgdn:associationId | lhgdn:association:59802 | lld:lhgdn |