middle temporal gyrus — IGVFSM4938TFTC

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            {
                "category": "mismatched status",
                "detail": "Preview tissue [IGVFSM4938TFTC](/tissues/IGVFSM4938TFTC/) has in progress subobject phenotype term [DOID_14330](/phenotype-terms/DOID_14330/).",
                "level": 30,
                "level_name": "INTERNAL_ACTION",
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            },
            {
                "category": "mismatched status",
                "detail": "Preview tissue [IGVFSM4938TFTC](/tissues/IGVFSM4938TFTC/) has in progress subobject phenotype term [DOID_9246](/phenotype-terms/DOID_9246/).",
                "level": 30,
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                "path": "/tissues/IGVFSM4938TFTC/"
            },
            {
                "category": "mismatched status",
                "detail": "Preview tissue [IGVFSM4938TFTC](/tissues/IGVFSM4938TFTC/) has in progress subobject phenotype term [DOID_0080832](/phenotype-terms/DOID_0080832/).",
                "level": 30,
                "level_name": "INTERNAL_ACTION",
                "name": "audit_item_status",
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            },
            {
                "category": "missing CCF ID",
                "detail": "Tissue [IGVFSM4938TFTC](/tissues/IGVFSM4938TFTC/) is missing a `ccf_id`. Human tissues are expected to specify a common coordinate framework identifier (CCF ID).",
                "level": 30,
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    "creation_timestamp": "2025-03-19T12:58:05.682251+00:00",
    "date_obtained": "2023-01-12",
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    "parts": [],
    "pmi": 208,
    "pmi_units": "minute",
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    "summary": "Homo sapiens (female, 80 years) middle temporal gyrus tissue associated with Parkinson's disease, cerebral amyloid angiopathy, mild cognitive impairment",
    "taxa": "Homo sapiens",
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}