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/genes/NEFH/genecombinations/?format=api
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/vnd.api+json
Vary: Accept

{
    "data": [
        {
            "type": "GeneCombination",
            "id": "294",
            "attributes": {
                "gene_relationship": [
                    "Monogenic experiments only",
                    "Relevant pathways for phenotype"
                ],
                "protein_interactions": [],
                "common_pathways": [
                    "Pathways of neurodegeneration - multiple diseases"
                ],
                "genecomb_metascore": 0,
                "lastmodified": "2021-10-18T11:01:00.969248"
            },
            "relationships": {
                "combination_set": {
                    "meta": {
                        "count": 1
                    },
                    "data": [
                        {
                            "type": "Combination",
                            "id": "OLI436"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/294/relationships/combination_set?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/294/combinations/?format=api"
                    }
                },
                "genes": {
                    "meta": {
                        "count": 2
                    },
                    "data": [
                        {
                            "type": "Gene",
                            "id": "NEFH"
                        },
                        {
                            "type": "Gene",
                            "id": "OPTN"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/294/relationships/genes?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/294/genes/?format=api"
                    }
                }
            },
            "links": {
                "self": "https://olida.ibsquare.be/api/genecombinations/294/?format=api"
            }
        },
        {
            "type": "GeneCombination",
            "id": "299",
            "attributes": {
                "gene_relationship": [
                    "Relevant pathways for phenotype"
                ],
                "protein_interactions": [],
                "common_pathways": [
                    "Pathways of neurodegeneration - multiple diseases"
                ],
                "genecomb_metascore": 0,
                "lastmodified": "2021-10-18T11:01:01.128556"
            },
            "relationships": {
                "combination_set": {
                    "meta": {
                        "count": 1
                    },
                    "data": [
                        {
                            "type": "Combination",
                            "id": "OLI441"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/299/relationships/combination_set?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/299/combinations/?format=api"
                    }
                },
                "genes": {
                    "meta": {
                        "count": 2
                    },
                    "data": [
                        {
                            "type": "Gene",
                            "id": "CHMP2B"
                        },
                        {
                            "type": "Gene",
                            "id": "NEFH"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/299/relationships/genes?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/299/genes/?format=api"
                    }
                }
            },
            "links": {
                "self": "https://olida.ibsquare.be/api/genecombinations/299/?format=api"
            }
        },
        {
            "type": "GeneCombination",
            "id": "601",
            "attributes": {
                "gene_relationship": [
                    "Involved in the same disease",
                    "Relevant pathways for phenotype"
                ],
                "protein_interactions": [],
                "common_pathways": [],
                "genecomb_metascore": 0,
                "lastmodified": "2021-10-18T11:01:18.231765"
            },
            "relationships": {
                "combination_set": {
                    "meta": {
                        "count": 1
                    },
                    "data": [
                        {
                            "type": "Combination",
                            "id": "OLI828"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/601/relationships/combination_set?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/601/combinations/?format=api"
                    }
                },
                "genes": {
                    "meta": {
                        "count": 2
                    },
                    "data": [
                        {
                            "type": "Gene",
                            "id": "GRN"
                        },
                        {
                            "type": "Gene",
                            "id": "NEFH"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/601/relationships/genes?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/601/genes/?format=api"
                    }
                }
            },
            "links": {
                "self": "https://olida.ibsquare.be/api/genecombinations/601/?format=api"
            }
        },
        {
            "type": "GeneCombination",
            "id": "1150",
            "attributes": {
                "gene_relationship": [
                    "Involved in the same disease",
                    "Relevant pathways for phenotype"
                ],
                "protein_interactions": [],
                "common_pathways": [],
                "genecomb_metascore": 1,
                "lastmodified": "2024-02-29T15:02:21.367646"
            },
            "relationships": {
                "combination_set": {
                    "meta": {
                        "count": 1
                    },
                    "data": [
                        {
                            "type": "Combination",
                            "id": "OLI1629"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/1150/relationships/combination_set?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/1150/combinations/?format=api"
                    }
                },
                "genes": {
                    "meta": {
                        "count": 2
                    },
                    "data": [
                        {
                            "type": "Gene",
                            "id": "ARHGEF28"
                        },
                        {
                            "type": "Gene",
                            "id": "NEFH"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/1150/relationships/genes?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/1150/genes/?format=api"
                    }
                }
            },
            "links": {
                "self": "https://olida.ibsquare.be/api/genecombinations/1150/?format=api"
            }
        },
        {
            "type": "GeneCombination",
            "id": "1159",
            "attributes": {
                "gene_relationship": [
                    "Involved in the same disease",
                    "Relevant pathways for phenotype"
                ],
                "protein_interactions": [],
                "common_pathways": [
                    "Amyotrophic lateral sclerosis"
                ],
                "genecomb_metascore": 2,
                "lastmodified": "2024-02-29T15:02:21.535070"
            },
            "relationships": {
                "combination_set": {
                    "meta": {
                        "count": 1
                    },
                    "data": [
                        {
                            "type": "Combination",
                            "id": "OLI1640"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/1159/relationships/combination_set?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/1159/combinations/?format=api"
                    }
                },
                "genes": {
                    "meta": {
                        "count": 2
                    },
                    "data": [
                        {
                            "type": "Gene",
                            "id": "HNRNPA2B1"
                        },
                        {
                            "type": "Gene",
                            "id": "NEFH"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/1159/relationships/genes?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/1159/genes/?format=api"
                    }
                }
            },
            "links": {
                "self": "https://olida.ibsquare.be/api/genecombinations/1159/?format=api"
            }
        },
        {
            "type": "GeneCombination",
            "id": "1214",
            "attributes": {
                "gene_relationship": [
                    "Involved in the same disease"
                ],
                "protein_interactions": [],
                "common_pathways": [
                    "Pathways of neurodegeneration - multiple diseases",
                    "Amyotrophic lateral sclerosis"
                ],
                "genecomb_metascore": 2,
                "lastmodified": "2024-02-29T15:02:22.676213"
            },
            "relationships": {
                "combination_set": {
                    "meta": {
                        "count": 1
                    },
                    "data": [
                        {
                            "type": "Combination",
                            "id": "OLI1704"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/1214/relationships/combination_set?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/1214/combinations/?format=api"
                    }
                },
                "genes": {
                    "meta": {
                        "count": 3
                    },
                    "data": [
                        {
                            "type": "Gene",
                            "id": "ALS2"
                        },
                        {
                            "type": "Gene",
                            "id": "NEFH"
                        },
                        {
                            "type": "Gene",
                            "id": "SPG11"
                        }
                    ],
                    "links": {
                        "self": "https://olida.ibsquare.be/api/genecombinations/1214/relationships/genes?format=api",
                        "related": "https://olida.ibsquare.be/api/genecombinations/1214/genes/?format=api"
                    }
                }
            },
            "links": {
                "self": "https://olida.ibsquare.be/api/genecombinations/1214/?format=api"
            }
        }
    ]
}