Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_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." NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_assertion evidence source_evidence_literature NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_assertion SIO_000772 18805825 NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_assertion wasDerivedFrom gad-20150221 NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_assertion wasGeneratedBy ECO_0000203 NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP126633.RAwT1kTU7eV6GmIdCs9o31qWrexPR6_zaqWtxzNv4A3dg130_provenance.