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/OLI273/references/?format=api
https://olida.ibsquare.be/api/references/790/relationships/combinations?format=api", "related": "https://olida.ibsquare.be/api/references/790/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/references/790/?format=api" } }, { "type": "Reference", "id": "831", "attributes": { "status": "CU", "pubmed_id": 32409511, "doi": "10.1136/jmedgenet-2020-106866", "pmc_id": null, "abstract": null, "year": 2020, "pdf": null, "comment": null, "uri": null, "bibtex": null, "title": "Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis", "lastmodified": "2021-11-16T17:59:55.860345" }, "relationships": { "combinations": { "meta": { "count": 14 }, "data": [ { "type": "Combination", "id": "OLI273" }, { "type": "Combination", "id": "OLI624" }, { "type": "Combination", "id": "OLI625" }, { "type": "Combination", "id": "OLI626" }, { "type": "Combination", "id": "OLI627" }, { "type": "Combination", "id": "OLI628" }, { "type": "Combination", "id": "OLI629" }, { "type": "Combination", "id": "OLI630" }, { "type": "Combination", "id": "OLI631" }, { "type": "Combination", "id": "OLI632" }, { "type": "Combination", "id": "OLI633" }, { "type": "Combination", "id": "OLI634" }, { "type": "Combination", "id": "OLI635" }, { "type": "Combination", "id": "OLI636" } ], "links": { "self": "https://olida.ibsquare.be/api/references/831/relationships/combinations?format=api", "related": "https://olida.ibsquare.be/api/references/831/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/references/831/?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": "790", "attributes": { "status": "CU", "pubmed_id": 25382069, "doi": "10.1002/ana.24306", "pmc_id": "PMC4293318", "abstract": null, "year": 2014, "pdf": null, "comment": null, "uri": null, "bibtex": null, "title": "Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes", "lastmodified": "2021-11-16T17:59:55.506750" }, "relationships": { "combinations": { "meta": { "count": 15 }, "data": [ { "type": "Combination", "id": "OLI269" }, { "type": "Combination", "id": "OLI270" }, { "type": "Combination", "id": "OLI271" }, { "type": "Combination", "id": "OLI272" }, { "type": "Combination", "id": "OLI273" }, { "type": "Combination", "id": "OLI274" }, { "type": "Combination", "id": "OLI275" }, { "type": "Combination", "id": "OLI276" }, { "type": "Combination", "id": "OLI277" }, { "type": "Combination", "id": "OLI278" }, { "type": "Combination", "id": "OLI279" }, { "type": "Combination", "id": "OLI280" }, { "type": "Combination", "id": "OLI281" }, { "type": "Combination", "id": "OLI282" }, { "type": "Combination", "id": "OLI283" } ], "links": { "self": "