Source:http://linkedlifedata.com/resource/lhgdn/association:18310
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:18310 | lhgdn:found_in | pubmed-article:16960802 | lld:lhgdn |
| lhgdn:association:18310 | lhgdn:geneRifSource | it is reported for the first time that mutations in CABP4 lead to autosomal recessive congenital stationary night blindness | lld:lhgdn |
| lhgdn:association:18310 | lhgdn:mesh_code | D009755 | lld:lhgdn |
| lhgdn:association:18310 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:18310 | lhgdn:umls_code | umls-concept:C0028077 | lld:mappings |
| entrez-gene:57010 | lhgdn:associationId | lhgdn:association:18310 | lld:lhgdn |