{
  "meta": {
    "data_length": 1,
    "message": "Proposition id prop:vtxr:413 retrieved successfully",
    "request_url": "http://api.moalmanac.org/propositions?proposition_id=prop%3Avtxr%3A413",
    "status": "success",
    "status_code": 200,
    "timestamp_elapsed": 0.0029,
    "timestamp_received": "2026-09-25T00:12:15.726890+00:00Z",
    "timestamp_returned": "2026-09-25T00:12:15.729790+00:00Z",
    "trace_id": "12c037e9-c114-4793-bc4f-3c7d8ee27541"
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    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
    "release": "draft",
    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-08-02"
  },
  "data": [
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      "id": "prop:vtxr:413",
      "type": "VariantTherapeuticResponseProposition",
      "predicate": "predictsSensitivityTo",
      "subjectVariant": {
        "type": "CategoricalVariant",
        "description": "Placeholder. Cat-VRS does not yet support sets of categorical variants. See the 'biomarkers' extension for biomarkers associated with this Proposition."
      },
      "conditionQualifier": {
        "id": "dis:oncotree:BRCA",
        "conceptType": "Disease",
        "name": "Invasive Breast Carcinoma",
        "mappings": [],
        "extensions": [
          {
            "name": "solid_tumor",
            "value": true,
            "description": "Boolean value for if this tumor type is categorized as a solid tumor."
          }
        ],
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          "code": "BRCA",
          "name": "Invasive Breast Carcinoma",
          "system": "https://oncotree.mskcc.org",
          "systemVersion": "oncotree_2021_11_02",
          "iris": [
            "https://oncotree.mskcc.org/?version=oncotree_2021_11_02&field=CODE&search=BRCA"
          ]
        }
      },
      "objectTherapeutic": {
        "id": "tx:ncit:C95733",
        "conceptType": "Therapy",
        "name": "Talazoparib",
        "mappings": [
          {
            "relation": "relatedMatch",
            "coding": {
              "id": "coding:rxcui:2099704",
              "code": "2099704",
              "name": "talazoparib",
              "system": "RxNorm",
              "systemVersion": "02-Mar-2026",
              "iris": [
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              ]
            }
          },
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            "relation": "relatedMatch",
            "coding": {
              "id": "coding:omop:35201068",
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              "name": "talazoparib",
              "system": "OMOP",
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              "iris": [
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            }
          },
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            "relation": "relatedMatch",
            "coding": {
              "id": "coding:sctid:782199007",
              "code": "782199007",
              "name": "Talazoparib",
              "system": "SNOMED",
              "systemVersion": "2025-03-01",
              "iris": [
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              ]
            }
          },
          {
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            "coding": {
              "id": "coding:omop:36684109",
              "code": "36684109",
              "name": "Talazoparib",
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              "iris": [
                "https://athena.ohdsi.org/search-terms/terms/36684109"
              ]
            }
          }
        ],
        "extensions": [
          {
            "name": "therapy_strategy",
            "value": [
              "PARP inhibition"
            ],
            "description": "Associated therapeutic strategy or mechanism of action of the therapy."
          },
          {
            "name": "therapy_type",
            "value": "Targeted therapy",
            "description": "Type of cancer treatment from cancer.gov: https://www.cancer.gov/about-cancer/treatment/types"
          }
        ],
        "primaryCoding": {
          "id": "coding:ncit:C95733",
          "code": "C95733",
          "name": "Talazoparib",
          "system": "https://evsexplore.semantics.cancer.gov",
          "systemVersion": "25.01d",
          "iris": [
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          ]
        }
      },
      "extensions": [
        {
          "name": "biomarkers",
          "value": [
            {
              "id": "bmkr.criterion:50",
              "present": true,
              "subject": {
                "id": "bmkr:50",
                "type": "CategoricalVariant",
                "name": "BRCA2 pathogenic variants",
                "constraints": [
                  {
                    "type": "DefiningLocationConstraint",
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                      "id": "ga4gh:SL.7RukGUDX8Q-lC8U7OIIL3hRCBfXr7tji",
                      "type": "SequenceLocation",
                      "name": null,
                      "aliases": [],
                      "description": "Sequence spanning the length of refseq:NP_000050.3, the protein product of the MANE Select coding transcript for BRCA2 (refseq:NM_000059.4).",
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                        "type": "SequenceReference",
                        "name": "NP_000050.3",
                        "aliases": [
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                          "ga4gh:SQ.A6rzuv6kdsuIp6gy6fykzgzyJe9NJOC9",
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                        ],
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                        "refgetAccession": "SQ.A6rzuv6kdsuIp6gy6fykzgzyJe9NJOC9",
                        "residueAlphabet": "aa"
                      },
                      "start": 0,
                      "end": 3418,
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                    },
                    "relations": [],
                    "matchCharacteristic": {
                      "primaryCoding": {
                        "code": "is_within",
                        "system": "ga4gh-gks-term:location-match"
                      }
                    }
                  },
                  {
                    "type": "FeatureContextConstraint",
                    "featureContext": {
                      "id": "gene:hgnc:1101",
                      "conceptType": "Gene",
                      "name": "BRCA2",
                      "primaryCoding": {
                        "id": "coding:hgnc:1101",
                        "code": "HGNC:1101",
                        "system": "https://genenames.org",
                        "iris": [
                          "https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:1101"
                        ]
                      },
                      "mappings": [
                        {
                          "relation": "exactMatch",
                          "coding": {
                            "id": "coding:ensembl:ensg00000139618",
                            "code": "ENSG00000139618",
                            "system": "https://www.ensembl.org",
                            "iris": [
                              "https://www.ensembl.org/id/ENSG00000139618"
                            ]
                          }
                        },
                        {
                          "relation": "exactMatch",
                          "coding": {
                            "id": "coding:ncbi:675",
                            "code": "675",
                            "system": "https://www.ncbi.nlm.nih.gov/gene",
                            "iris": [
                              "https://www.ncbi.nlm.nih.gov/gene/675"
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                          }
                        },
                        {
                          "relation": "relatedMatch",
                          "coding": {
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                            "code": "NM_000059.4",
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                            "iris": [
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                        }
                      ]
                    }
                  }
                ],
                "extensions": [
                  {
                    "name": "biomarker_type",
                    "value": "Germline variant"
                  },
                  {
                    "name": "chromosome",
                    "value": "13"
                  },
                  {
                    "name": "start_position",
                    "value": null
                  },
                  {
                    "name": "end_position",
                    "value": null
                  },
                  {
                    "name": "reference_allele",
                    "value": null
                  },
                  {
                    "name": "alternate_allele",
                    "value": null
                  },
                  {
                    "name": "cdna_change",
                    "value": null
                  },
                  {
                    "name": "protein_change",
                    "value": null
                  },
                  {
                    "name": "variant_annotation",
                    "value": null
                  },
                  {
                    "name": "exon",
                    "value": null
                  },
                  {
                    "name": "rsid",
                    "value": null
                  },
                  {
                    "name": "hgvsg",
                    "value": null
                  },
                  {
                    "name": "hgvsc",
                    "value": null
                  },
                  {
                    "name": "requires_pathogenic",
                    "value": true
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                ]
              }
            },
            {
              "id": "bmkr.criterion:2",
              "present": true,
              "subject": {
                "id": "bmkr:2",
                "type": "CategoricalVariant",
                "name": "HER2-negative",
                "constraints": [],
                "extensions": [
                  {
                    "name": "biomarker_type",
                    "value": "Protein expression"
                  },
                  {
                    "name": "marker",
                    "value": "Human epidermal growth factor receptor 2 (HER2)"
                  },
                  {
                    "name": "unit",
                    "value": "status"
                  },
                  {
                    "name": "equality",
                    "value": "="
                  },
                  {
                    "name": "value",
                    "value": "Negative"
                  }
                ]
              }
            }
          ],
          "description": "The biomarkers associated with this Proposition, each with a `present` flag indicating if the biomarker is present (true) or absent (false). Multiple biomarkers are combined with implied AND logic."
        }
      ]
    }
  ]
}