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/references/?format=api
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"comment": null, "uri": null, "bibtex": null, "title": "Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy", "lastmodified": "2021-11-16T17:59:54.777186" }, "relationships": { "combinations": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI068" } ], "links": { "self": "https://olida.ibsquare.be/api/references/610/relationships/combinations?format=api", "related": "https://olida.ibsquare.be/api/references/610/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/references/610/?format=api" } }, { "type": "Reference", "id": "611", "attributes": { "status": "CU", "pubmed_id": 31073086, "doi": "10.1183/13993003.02041-2018", "pmc_id": "PMC6637284", "abstract": null, "year": 2019, "pdf": null, "comment": null, "uri": null, "bibtex": null, "title": "An atypical pulmonary fibrosis is associated with co-inheritance of mutations in the calcium binding protein genes S100A3 and S100A13", "lastmodified": "2021-11-16T17:59:54.779600" }, "relationships": { "combinations": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI074" } ], "links": { "self": "https://olida.ibsquare.be/api/references/611/relationships/combinations?format=api", "related": "https://olida.ibsquare.be/api/references/611/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/references/611/?format=api" } }, { "type": "Reference", "id": "612", "attributes": { "status": "CU", "pubmed_id": 29255181, "doi": "10.1038/s41431-017-0014-1", "pmc_id": "PMC5865213", "abstract": null, "year": 2017, "pdf": null, "comment": null, "uri": null, "bibtex": null, "title": "Next-generation sequencing of patients with congenital anosmia", "lastmodified": "2021-11-16T17:59:54.781398" }, "relationships": { "combinations": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI075" } ], "links": { "self": 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DUOX2 Mutations in Cases With Congenital Hypothyroidism", "lastmodified": "2021-11-16T17:59:54.789292" }, "relationships": { "combinations": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI040" } ], "links": { "self": "https://olida.ibsquare.be/api/references/616/relationships/combinations?format=api", "related": "https://olida.ibsquare.be/api/references/616/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/references/616/?format=api" } }, { "type": "Reference", "id": "617", "attributes": { "status": "CU", "pubmed_id": 12677556, "doi": "10.1086/375178", "pmc_id": "PMC1180271", "abstract": null, "year": 2003, "pdf": null, "comment": null, "uri": null, "bibtex": null, "title": "Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome", "lastmodified": "2021-11-16T17:59:54.791253" }, "relationships": { "combinations": { "meta": { "count": 7 }, "data": [ { "type": 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