Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_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." NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_assertion evidence source_evidence_literature NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_assertion SIO_000772 15685536 NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_assertion wasDerivedFrom gad-20150221 NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_assertion wasGeneratedBy ECO_0000203 NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP64238.RAMxtdoIpEEyeWFYMoBODit0X11HpDhC0HuQ3uUsuN_cU130_provenance.