rewirebio.iobenchmarks
Evidence claim

popEVE: description

Description of popEVE

Deep generative model that combines evolutionary and human population data to score variant deleteriousness on a scale calibrated across the proteome.

Replace a category-only description with a sourced functional description (issue #88). Historical releases retain the original value.

Evidence

Source checking verifies the cited claim or transcription. It does not establish independent reproduction.

Evidence table

Inspect claims, sources and review details

Trace each statement to its source and review. A context-only reference supports the record generally; it does not verify an individual field. Source checking does not reproduce an experiment.

One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.

7 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-10-22-1b7cf027e4f6
Property and statementOriginal source and locationReview and provenance
Claimed field
description
Context-only references
Proteome-wide model for human disease genetics (popEVE)

Original source ↗

qa-descriptions-20261011-e-source-popeve: Abstract

Version: Europe PMC full-text XML for PMC12695638, Nature Genetics 2025
Retrieved: 2026-10-11T01:38:40Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.field

Source artifact SHA-256: 5995c0b15ea643adfbc7123beb9a9017aca518e4052c92088a5b5ae26e7781be

Hash scope: SHA-256 of one retrieval of the Europe PMC full-text XML. These renderings are not always byte-stable; the article text is the evidence.

Inspected artifact

Previous value
Variant effect predictor for missense variants.
Context-only references
Proteome-wide model for human disease genetics (popEVE)

Original source ↗

qa-descriptions-20261011-e-source-popeve: Abstract

Version: Europe PMC full-text XML for PMC12695638, Nature Genetics 2025
Retrieved: 2026-10-11T01:38:40Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.previous_value

Source artifact SHA-256: 5995c0b15ea643adfbc7123beb9a9017aca518e4052c92088a5b5ae26e7781be

Hash scope: SHA-256 of one retrieval of the Europe PMC full-text XML. These renderings are not always byte-stable; the article text is the evidence.

Inspected artifact

Source location
qa-descriptions-20261011-e-source-popeve: Abstract
Context-only references
Proteome-wide model for human disease genetics (popEVE)

Original source ↗

qa-descriptions-20261011-e-source-popeve: Abstract

Version: Europe PMC full-text XML for PMC12695638, Nature Genetics 2025
Retrieved: 2026-10-11T01:38:40Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.source_locator

Source artifact SHA-256: 5995c0b15ea643adfbc7123beb9a9017aca518e4052c92088a5b5ae26e7781be

Hash scope: SHA-256 of one retrieval of the Europe PMC full-text XML. These renderings are not always byte-stable; the article text is the evidence.

Inspected artifact

Claimed value
Deep generative model that combines evolutionary and human population data to score variant deleteriousness on a scale calibrated across the proteome.
Context-only references
Proteome-wide model for human disease genetics (popEVE)

Original source ↗

qa-descriptions-20261011-e-source-popeve: Abstract

Version: Europe PMC full-text XML for PMC12695638, Nature Genetics 2025
Retrieved: 2026-10-11T01:38:40Z

not individually reviewed

No individual claim review recorded

Audit details

Field: attributes.value

Source artifact SHA-256: 5995c0b15ea643adfbc7123beb9a9017aca518e4052c92088a5b5ae26e7781be

Hash scope: SHA-256 of one retrieval of the Europe PMC full-text XML. These renderings are not always byte-stable; the article text is the evidence.

Inspected artifact

Description
Replace a category-only description with a sourced functional description (issue #88). Historical releases retain the original value.
Context-only references
Proteome-wide model for human disease genetics (popEVE)

Original source ↗

qa-descriptions-20261011-e-source-popeve: Abstract

Version: Europe PMC full-text XML for PMC12695638, Nature Genetics 2025
Retrieved: 2026-10-11T01:38:40Z

not individually reviewed

No individual claim review recorded

Audit details

Field: description

Source artifact SHA-256: 5995c0b15ea643adfbc7123beb9a9017aca518e4052c92088a5b5ae26e7781be

Hash scope: SHA-256 of one retrieval of the Europe PMC full-text XML. These renderings are not always byte-stable; the article text is the evidence.

Inspected artifact

Relationship: subject
somatic-oncogenicity-20261009-method-popeve
Context-only references
Proteome-wide model for human disease genetics (popEVE)

Original source ↗

qa-descriptions-20261011-e-source-popeve: Abstract

Version: Europe PMC full-text XML for PMC12695638, Nature Genetics 2025
Retrieved: 2026-10-11T01:38:40Z

not individually reviewed

No individual claim review recorded

Audit details

Field: links:subject:somatic-oncogenicity-20261009-method-popeve

Source artifact SHA-256: 5995c0b15ea643adfbc7123beb9a9017aca518e4052c92088a5b5ae26e7781be

Hash scope: SHA-256 of one retrieval of the Europe PMC full-text XML. These renderings are not always byte-stable; the article text is the evidence.

Inspected artifact

Name
popEVE: description
Context-only references
Proteome-wide model for human disease genetics (popEVE)

Original source ↗

qa-descriptions-20261011-e-source-popeve: Abstract

Version: Europe PMC full-text XML for PMC12695638, Nature Genetics 2025
Retrieved: 2026-10-11T01:38:40Z

not individually reviewed

No individual claim review recorded

Audit details

Field: name

Source artifact SHA-256: 5995c0b15ea643adfbc7123beb9a9017aca518e4052c92088a5b5ae26e7781be

Hash scope: SHA-256 of one retrieval of the Europe PMC full-text XML. These renderings are not always byte-stable; the article text is the evidence.

Inspected artifact

Sources and history

Release 2026-10-22-1b7cf027e4f6 · Record review: source checked

1 source record and release historyDownload this release (gzip)
Technical metadata and extraction receipts

Stable ID: metadata-correction-edda4c75f5b01ddb5028

areas
dna-genomes
contexts
clinical_research
method types
specialist
field
description
previous value
Variant effect predictor for missense variants.
value
Deep generative model that combines evolutionary and human population data to score variant deleteriousness on a scale calibrated across the proteome.
source locator
qa-descriptions-20261011-e-source-popeve: Abstract
review
method: automated-source-review; ai-assisted-source-review; reviewer: claude; reviewer note: Extractor: Claude integrator agent for issue #88. Reviewer: a separate Claude review agent, independent of the extractor; no human review claimed.; date: 2026-10-11; method note: Compared the store diff with origin/main, read each new description against its cited source passage and checked the licence of each new source record.; note: Approved with two corrections, both applied: the MutFormer source licence is CC BY 4.0 per the arXiv abstract page, and the MetaRNN source locator now names the Background passage. Checked the 27 Chen 2020 descriptions row by row against Table 1 (PMC7033911) and spot-checked AlphaMissense, MisFit, popEVE, VARITY, MetaRNN, MutFormer and gMVP against their abstracts; accurate. Licences on the other new sources match Europe PMC.; receipt: data/omics/qa-descriptions-20261011-e/review.json
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