Source:http://linkedlifedata.com/resource/lhgdn/association:59213
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:59213 | lhgdn:found_in | pubmed-article:12471201 | lld:lhgdn |
lhgdn:association:59213 | lhgdn:geneRifSource | Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t (6; 13) (q21; q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype | lld:lhgdn |
lhgdn:association:59213 | lhgdn:mesh_code | D008831 | lld:lhgdn |
lhgdn:association:59213 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:59213 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
entrez-gene:8724 | lhgdn:associationId | lhgdn:association:59213 | lld:lhgdn |