Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_assertion wasGeneratedBy ECO_0000203 NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_assertion wasDerivedFrom befree-20140225 NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_assertion SIO_000772 23850713 NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_assertion evidence source_evidence_literature NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_assertion description "[Further analysis of the 11q13 locus revealed a non-synonymous single nucleotide polymorphism (SNP) (R220W/rs11235604) in the evolutionarily conserved region of ATG16L2 with stronger association (OR=1.61, combined p=2.44×10(-12)) than rs11235667, suggesting ATG16L2 as a novel susceptibility gene for CD and rs11235604 to be a potential causal variant of the association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP381572.RADSuRFWCK1jh6rcnZOoT6zGufTKEOnIt3Wm9z0OnBiKI130_provenance.