Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_assertion description "[Common variation in IL2/IL21, RGS1, IL12A/SCHIP and SH2B3 was associated with susceptibility to CD in our Italian cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_assertion evidence source_evidence_literature NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_assertion SIO_000772 18805825 NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_assertion wasDerivedFrom befree-20150227 NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_assertion wasGeneratedBy ECO_0000203 NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP505677.RABqEg1DISDkVXYAT2Py0Vgz9RswmOG78fGeUKunG3VYw130_provenance.