Reference List
This API endpoint handles listing (/references) and retrieval (/references/<ID>/) of References from the database
that support the inclusion of at least one oligogenic combination in OLIDA.
GET /api/combinations/OLI1018/references/?format=api
https://olida.ibsquare.be/api/references/893/relationships/combinations?format=api", "related": "https://olida.ibsquare.be/api/references/893/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/references/893/?format=api" } }, { "type": "Reference", "id": "897", "attributes": { "status": "CU", "pubmed_id": 22232210, "doi": "10.1172/JCI59526", "pmc_id": "PMC3266790", "abstract": null, "year": 2012, "pdf": null, "comment": null, "uri": null, "bibtex": null, "title": "Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver", "lastmodified": "2022-08-04T14:15:51.852309" }, "relationships": { "combinations": { "meta": { "count": 2 }, "data": [ { "type": "Combination", "id": "OLI1017" }, { "type": "Combination", "id": "OLI1018" } ], "links": { "self": "https://olida.ibsquare.be/api/references/897/relationships/combinations?format=api", "related": "https://olida.ibsquare.be/api/references/897/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/references/897/?format=api" } } ], "meta": { "database_name": "OLIgogenic diseases DAtabase (OLIDA)", "resource_url": "olida.ibsquare.be", "api_release_year": "2021", "api_developer": [ [ "Arnau Dillen", "arnau.dillen@ulb.ac.be" ], [ "Charlotte Nachtegael", "charlotte.nachtegael@ulb.be" ] ], "api_version": "0.3", "api_maintainers": [ [ "Charlotte Nachtegael", "charlotte.nachtegael@ulb.be" ] ], "api_documentation": [ "olida.ibsquare.be/api/swagger", "olida.ibsquare.be/api/redoc" ], "copyright": "Copyright (c) 2025 · OLIDA All Rights Reserved.", "license": "CC Attribution-NonCommercial 4.0 International License", "ontologies": { "ORDO": "http://bioportal.bioontology.org/ontologies/ORDO", "GENO": "http://purl.obolibrary.org/obo/geno.owl", "MI": "http://purl.obolibrary.org/obo/mi.owl", "NCIT": "http://purl.obolibrary.org/obo/ncit.owl", "OGI": "http://purl.obolibrary.org/obo/ogi.owl", "OGG": "http://purl.obolibrary.org/obo/ogg.owl" }, "relevant_publications_doi": [ "10.1093/nar/gkv1068", "10.1093/database/baac023" ], "size": 2 } }{ "data": [ { "type": "Reference", "id": "893", "attributes": { "status": "CU", "pubmed_id": 25546334, "doi": "10.1002/humu.22745", "pmc_id": null, "abstract": null, "year": 2015, "pdf": null, "comment": null, "uri": null, "bibtex": null, "title": "Recessive Inheritance of Population-Specific Intronic LINE-1 Insertion Causes a Rotor Syndrome Phenotype", "lastmodified": "2022-08-04T14:15:51.716766" }, "relationships": { "combinations": { "meta": { "count": 2 }, "data": [ { "type": "Combination", "id": "OLI1007" }, { "type": "Combination", "id": "OLI1018" } ], "links": { "self": "