Version history

1 version on record. Newest first; the live version sits at the top with a live indicator.

  1. Live c8028328dca0
    5/17/2026, 4:35:28 PM
    Content snapshot
    {
      "scope": "vip-interneurons",
      "claim_text": "Developmental loss of MeCP2 from VIP interneurons impairs cortical function and Rett-like behaviors",
      "raw_fields": {
        "n": null,
        "doi": "10.7554/elife.55639",
        "pmid": "32343226",
        "tags": [
          "snowball_fwd"
        ],
        "year": "2020",
        "claim": "Developmental loss of MeCP2 from VIP interneurons impairs cortical function and Rett-like behaviors",
        "pmcid": "PMC7213975",
        "round": 2,
        "title": "Developmental loss of MeCP2 from VIP interneurons impairs cortical function and behavior",
        "journal": "eLife",
        "citation": "James M. Mossner; Renata Batista‐Brito; Rima Pant; Jessica A. Cardin",
        "cite_key": "Mossner2020",
        "effect_size": null,
        "text_access": "fulltext",
        "citedByCount": 59,
        "isOpenAccess": "Y",
        "evidence_type": "mechanism",
        "linked_topics": [
          "snowball_fwd"
        ],
        "_source_cluster": "cluster_07_in_vivo_function",
        "relevance_score": 0.8,
        "replication_status": null,
        "_source_cluster_index": 55,
        "claim_source_sentence": "Rett Syndrome is a devastating neurodevelopmental disorder resulting from mutations in the gene <i>MECP2</i>."
      },
      "section_id": "section_13",
      "source_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP/blob/95e761177f7d2ec565983d3307c14ec238f9677c/evidence/section_13_evidence_package.json",
      "effect_size": null,
      "review_repo": "ComputationalReviewVIP",
      "section_ref": "wiki_page:computationalreviewvip-13-conclusion",
      "source_kind": "review_finding",
      "source_path": "evidence/section_13_evidence_package.json",
      "source_refs": [
        "paper:paper-4effa559f79e"
      ],
      "source_span": "Rett Syndrome is a devastating neurodevelopmental disorder resulting from mutations in the gene <i>MECP2</i>.",
      "study_system": null,
      "evidence_refs": [
        {
          "ref": "paper:paper-4effa559f79e"
        }
      ],
      "section_title": "Synthesis and Conclusion: Reassessing the Canonical VIP Disinhibitor",
      "source_policy": {
        "mode": "public_source_pointer_with_short_context",
        "notes": [
          "Local review repositories are read-only inputs.",
          "SciDEX stores paper metadata, structured evidence, file pointers, and short citation contexts; it does not copy full review prose."
        ],
        "source_commit_sha": "95e761177f7d2ec565983d3307c14ec238f9677c",
        "source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP"
      },
      "evidence_summary": null,
      "review_bundle_ref": "analysis_bundle:ab-2ce40c33e827",
      "replication_status": "unevaluated",
      "review_package_ref": "analysis_bundle:ab-2ce40c33e827",
      "source_artifact_ref": "wiki_page:computationalreviewvip-13-conclusion",
      "origin_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP/blob/95e761177f7d2ec565983d3307c14ec238f9677c/evidence/section_13_evidence_package.json",
      "commit_sha": "95e761177f7d2ec565983d3307c14ec238f9677c",
      "created_by": "persona-jerome-lecoq-gbo-neuroscience",
      "repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP"
    }