Bibliographic record
Abstract
目的探讨中国湖南籍汉族强直性脊柱炎(AS)患者人群中,TNF-α-857位C→T基因突变与AS的相关性,及其致病的可能分子生物学机制。方法在164例AS患者和121名正常对照中,用等位基因特异性扩增的方法,对TNF-α基因启动子-857C/T单核苷酸多态性(single nucleotide polymor-phisms,SNPs)进行基因分型,分析单个位点的等位基因和基因型频率是否与AS相关。结果AS患者组TNF-α-857T的等位基因频率(P=0.002)和基因型频率(P=0.000002)均显著超过正常对照组,经Bon-ferroni校正后仍为阳性。结论本研究显示TNF-α-857基因多态性与AS存在显著的相关性,TNF-α-857T可能增加AS的易感性。
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.001 | 0.001 |
| Meta-epidemiology (narrow) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.001 |
| Bibliometrics | 0.001 | 0.000 |
| Science and technology studies | 0.001 | 0.001 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.001 | 0.001 |
| Insufficient payload (model declined to judge) | 0.006 | 0.001 |
Machine scores (provisional)
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.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".