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4,299,418 works, Canadian by any of four routes.

Every filter state is a URL; the URL is the query; the query is citable via /q/⟨hash⟩. The page, the API and the export parse the same parameters.

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The current cohort, streamed from the database: every work column, the machine labels, the provisional scores, and the per-row validation status. Exports are capped at 100,000 rows. Mints a permanent /q/ link for this exact query. The same filters always produce the same link, whoever asks.

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Orphanet Journal of Rare Diseases
Topic
Retraction
Abstract
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Label agreement
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Direct Codex and Gemma labels are unvalidated and sparse. Distilled predictions cover the full frame and are also unvalidated. Choose the evidence source explicitly; absence of a direct label is never a negative label.

affaffiliation
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The four routes compose: require the funder route and exclude affiliation to get the funder-only stratum no affiliation-based frame ever sees.

328 results · 1 filter active ·
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20062025
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Machine labels · sparse coverage
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An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
328 works in the cohort · of 4,299,418page 3 of 7

Labels cover 0 of 328 works in this cohort. The rest are unlabeled, which is not a negative label: the label table is sparse today and grows as labeling rounds land.

Distilled predictions cover 328 of 328 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundunlabeled
A generalizable pre-clinical research approach for orphan disease therapy
Chandree L. Beaulieu, Mark E. Samuels, Sean Ekins, Christopher R. McMaster, A.M. Edwards, Adrian R. Krainer +4 more
2012· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
34
citations
afffundunlabeled
Using a meta-narrative literature review and focus groups with key stakeholders to identify perceived challenges and solutions for generating robust evidence on the effectiveness of treatments for rare diseases
Kylie Tingley, Doug Coyle, Ian D. Graham, Lindsey Sikora, Pranesh Chakraborty, Kumanan Wilson +3 more
2018· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
32
citations
affunlabeled
Registries for orphan drugs: generating evidence or marketing tools?
Carla E. M. Hollak, Sandra Sirrs, Sibren van den Berg, Vincent van der Wel, Mirjam Langeveld, Hanka Dekker +2 more
2020· article· en· Orphanet Journal of Rare Diseases· Economics, Econometrics and Finance
distilled prediction:candidate · metaresearch+insufficient_payloadconsensus · none
28
citations
fundno affunlabeled
An ontological foundation for ocular phenotypes and rare eye diseases
Panagiotis I. Sergouniotis, Emmanuel Maxime, Dorothée Leroux, Annie Olry, Rachel Thompson, Ana Rath +2 more
2019· letter· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
26
citations
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