Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses
Primary source retrieved and hashed for the rare-disease reanalysis use-case pass.
Evidence
Source checking verifies the cited claim or transcription. It does not establish independent reproduction.
Evidence table
Inspect claims, sources and review details
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One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.
20 evidence rows matching the loaded filters
| Property and statement | Original source and location | Review and provenance |
|---|---|---|
| attributes.artifact_sha256 8bd0d50c0f3a1018c1f5ada9088a748d27d787eb5598e9857d2ddede85854ce6 Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.artifact_url https://www.ebi.ac.uk/europepmc/webservices/rest/PMC11513043/fullTextXML Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.doi 10.1038/s41525-024-00436-6 Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.licence CC-BY-4.0 Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.media_type application/xml Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.publication_status peer_reviewed Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.retrieved_at 2026-10-09T20:40:13Z Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.source_locator Licence statement in the article XML <license> element: Creative Commons Attribution 4.0 Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.url https://doi.org/10.1038/s41525-024-00436-6 Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
| attributes.venue npj Genomic Medicine Source metadata | Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses No field-specific location recorded Version: npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML | catalogued No individual claim review recorded Audit detailsField: Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
Sources and history
Release 2026-10-10-7fcc3e48a123 · Record review: source checked
Technical metadata and extraction receipts
Stable ID: rare-reanalysis-20261009-source-demidov2024
- areas
- dna-genomes
- contexts
- clinical_research
- url
- https://doi.org/10.1038/s41525-024-00436-6
- artifact url
- https://www.ebi.ac.uk/europepmc/webservices/rest/PMC11513043/fullTextXML
- version
- npj Genomic Medicine 9:49, published online 2024-10-26; PMC11513043 full-text XML
- retrieved at
- 2026-10-09T20:40:13Z
- artifact sha256
- 8bd0d50c0f3a1018c1f5ada9088a748d27d787eb5598e9857d2ddede85854ce6
- doi
- 10.1038/s41525-024-00436-6
- publication status
- peer_reviewed
- licence
- CC-BY-4.0
- media type
- application/xml
- venue
- npj Genomic Medicine
- year
- 2024
- source locator
- Licence statement in the article XML <license> element: Creative Commons Attribution 4.0