{
  "data": [
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      "assertionMethod": {
        "type": "VariantPathogenicityInterpretationGuideline"
      },
      "condition": {
        "@id": "https://api.monarchinitiative.org/api/bioentity/phenotype/MONDO:0004994",
        "id": "MONDO:0004994",
        "label": "cardiomyopathy",
        "type": "GeneticCondition"
      },
      "evidenceLine": [
        {
          "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA014901/MONDO:0004994/002/el/0/1747",
          "evidenceItem": [
            {
              "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA014901/MONDO:0004994/002/ei/1/1748",
              "contribution": [
                {
                  "agent": {
                    "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50002_EP155190197442076",
                    "id": "CG-PCER-AGENT:CG_50002_EP155190197442076",
                    "type": "Agent"
                  },
                  "contributionDate": {
                    "date": "2018/11/16",
                    "description": "Date on which this evidence was provided"
                  },
                  "contributionRole": {
                    "@id": "https://obofoundry.org/sepio/0000156",
                    "id": "SEPIO:0000516",
                    "label": "curator role",
                    "type": "ContributoryRole"
                  },
                  "type": "Contribution"
                }
              ],
              "evidenceLine": [
                {
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                            "id": "CG-PCER-AGENT:CG_50002_EP155190197442076",
                            "type": "Agent"
                          },
                          "comments": "Tools predict damaging",
                          "contributionDate": {
                            "date": "2018/11/16",
                            "description": "Date on which this evidence was provided"
                          },
                          "contributionRole": {
                            "@id": "https://obofoundry.org/sepio/0000156",
                            "id": "SEPIO:0000516",
                            "label": "curator role",
                            "type": "ContributoryRole"
                          },
                          "type": "Contribution"
                        }
                      ],
                      "id": "CA014901/MONDO:0004994/002/ci/CA014901/MONDO:0004994/002.002",
                      "type": "InfFromBkgrndSciKnow"
                    }
                  ],
                  "id": "CG-PCER-VARINT:CA014901/MONDO:0004994/002/0/1747/1749",
                  "type": "EvidenceLine"
                }
              ],
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              "statementOutcome": {
                "@id": "SEPIO:0000224",
                "label": "Met"
              },
              "type": "CriterionAssessment"
            }
          ],
          "evidenceStrength": {
            "@id": "https://obofoundry.org/sepio"
          },
          "id": "CG-PCER-VARINT:CA014901/MONDO:0004994/002/0/1747",
          "type": "EvidenceLine"
        },
        {
          "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA014901/MONDO:0004994/002/el/0/1804",
          "evidenceItem": [
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              "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA014901/MONDO:0004994/002/ei/1/1805",
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                    "id": "CG-PCER-AGENT:CG_50002_EP155190197442076",
                    "type": "Agent"
                  },
                  "contributionDate": {
                    "date": "2018/11/16",
                    "description": "Date on which this evidence was provided"
                  },
                  "contributionRole": {
                    "@id": "https://obofoundry.org/sepio/0000156",
                    "id": "SEPIO:0000516",
                    "label": "curator role",
                    "type": "ContributoryRole"
                  },
                  "type": "Contribution"
                }
              ],
              "evidenceLine": [
                {
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                  "evidenceItem": [
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                      "contribution": [
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                            "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50002_EP155190197442076",
                            "id": "CG-PCER-AGENT:CG_50002_EP155190197442076",
                            "type": "Agent"
                          },
                          "comments": "Filtering allele frequency of 0.0375% in Europeans in ExAC",
                          "contributionDate": {
                            "date": "2018/11/16",
                            "description": "Date on which this evidence was provided"
                          },
                          "contributionRole": {
                            "@id": "https://obofoundry.org/sepio/0000156",
                            "id": "SEPIO:0000516",
                            "label": "curator role",
                            "type": "ContributoryRole"
                          },
                          "type": "Contribution"
                        }
                      ],
                      "id": "CA014901/MONDO:0004994/002/ci/CA014901/MONDO:0004994/002.002",
                      "type": "InfFromBkgrndSciKnow"
                    }
                  ],
                  "id": "CG-PCER-VARINT:CA014901/MONDO:0004994/002/0/1804/1806",
                  "type": "EvidenceLine"
                }
              ],
              "id": "CG-PCER-VARINT:CA014901/MONDO:0004994/002/1/1805",
              "statementOutcome": {
                "@id": "SEPIO:0000224",
                "label": "Met"
              },
              "type": "CriterionAssessment"
            }
          ],
          "evidenceStrength": {
            "@id": "https://obofoundry.org/sepio"
          },
          "id": "CG-PCER-VARINT:CA014901/MONDO:0004994/002/0/1804",
          "type": "EvidenceLine"
        }
      ],
      "id": "CG-PCER-VARINT:CA014901/MONDO:0004994/002",
      "metadata": {
        "created": "2024-09-27T19:42:39.762Z",
        "note": "DISCLAIMER: While the data/content in this document is approved by ClinGen expert panel(s), the SEPIO schema presented here is an initial prototype and has not been reviewed nor finalized by the ClinGen Data Exchange Modeling Team. We expect it to differ significantly from the final schema.",
        "producedAtUTC": "Fri, 27 Sep 2024 19:42:39 -0000",
        "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
        "version": "1.0.0"
      },
      "statementOutcome": {
        "@id": "https://loinc.org/LA26334-5",
        "id": "LN:LA26334-5",
        "label": "Likely Benign"
      },
      "type": "VariantPathogenicityInterpretation",
      "uuid": "dfd5170f-2105-4cc6-870a-2f7511d716cd",
      "variant": {
        "@id": "https://reg.genome.network/allele/CA014901",
        "id": "CAR:CA014901",
        "relatedContextualAllele": [
          {
            "alleleName": [
              {
                "name": "NM_000257.3:c.4377G>T"
              }
            ],
            "preferred": true
          }
        ],
        "relatedIdentifier": [
          {
            "label": "NM_000257.3(MYH7):c.4377G>T (p.Lys1459Asn)"
          }
        ],
        "type": "CAR"
      }
    }
  ],
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-04-03T19:09:15.213Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}