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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.
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Phenotype
Crohn disease
435articles
435mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60NOD2/CARD15 polymorphisms (P268S, IVS8+158, G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study.
PMID 34341249 | PMCID PMC8448012 | DOI 10.4103/sjg.sjg_613_20 · Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association · 2021 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | Crohn disease | “NOD2/CARD15 polymorphisms (P268S, IVS8+158, G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study.” | 0.93 | phenotype_alias_lexicon_v2 |
| variant | IVS8+158 | “NOD2/CARD15 polymorphisms (P268S, IVS8+158, G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study.” | 0.82 | literature_variant_regex_v2 |
| gene | NOD2 | “NOD2/CARD15 polymorphisms (P268S, IVS8+158, G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study.” | 0.98 | hgnc_dict_v1 |
| variant | P268S | “NOD2/CARD15 polymorphisms (P268S, IVS8+158, G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study.” | 0.82 | literature_variant_regex_v2 |