Source:http://linkedlifedata.com/resource/lhgdn/association:2092
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:2092 | lhgdn:found_in | pubmed-article:12093833 | lld:lhgdn |
| lhgdn:association:2092 | lhgdn:geneRifSource | Patients affected by premature ovarian failure for the missense mutation (769G-- > A transition) in the exon 2 of the INHalpha gene. | lld:lhgdn |
| lhgdn:association:2092 | lhgdn:mesh_code | D016649 | lld:lhgdn |
| lhgdn:association:2092 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:2092 | lhgdn:umls_code | umls-concept:C0085215 | lld:mappings |
| entrez-gene:3623 | lhgdn:associationId | lhgdn:association:2092 | lld:lhgdn |