Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_assertion> ?p ?o ?g. }
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- NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_assertion type Assertion NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_head.
- NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_assertion description "[Phenotype-genotype associations were evaluated in a Canadian cohort including 507 patients with CD, 216 patients with UC, and 352 ethnically matched controls genotyped for SLC22A4 C1672T, SLC22A5 G-207C, and the major CD-associated CARD15 variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_provenance.
- NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_assertion evidence source_evidence_literature NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_provenance.
- NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_assertion SIO_000772 15685536 NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_provenance.
- NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_assertion wasDerivedFrom gad-20150221 NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_provenance.
- NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_assertion wasGeneratedBy ECO_0000203 NP64279.RAZD6djqiCpG8fnlcD2B_vokmXfCr59mD7CVl3xzRgl2U130_provenance.