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Functional variants of OCTN cation transporter genes are associated with Crohn disease

2004· article· en· 844 citations· W2096063169 on OpenAlex· 10.1038/ng1339

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

Machine scores (provisional)

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Opus teacher head0.009
GPT teacher head0.222
Teacher spread
0.214 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

No abstract. This is not a gap in this database — OpenAlex has none either. 23.3% of the frame is in this state, and the screen finds HALF as much metaresearch here, so the absence is a measured bias rather than a missing field.

The record

Venue
Nature Genetics
Topic
Drug Transport and Resistance Mechanisms
Field
Medicine
Canadian institutions
Hospital for Sick ChildrenOccupational Cancer Research CentreMount Sinai HospitalLunenfeld-Tanenbaum Research InstituteSt. Michael's HospitalAlethia Biotherapeutics (Canada)University Health NetworkSickKids FoundationUniversity of Toronto
Funders
National Institutes of HealthUniversity of TorontoCanadian Arthritis NetworkArthritis SocietyCrohn's and Colitis FoundationCrohn's and Colitis Foundation of CanadaCanadian Institutes of Health ResearchGenome Canada
Keywords
Crohn's diseaseBiologyHaplotypeSingle-nucleotide polymorphismGeneticsLocus (genetics)DiseaseGeneGenotypeInternal medicineMedicine
Has abstract in OpenAlex
no