Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_assertion description "[CD susceptibility polymorphisms ATG16L1 rs2241880, ICAM1 rs5498, IL4 rs2070874, IL17F rs763780, IRGM rs13361189, ITLN1 rs2274910, LRRK2 rs11175593, and TLR4 rs4986790 were genotyped in a Portuguese population (511 CD patients, 626 controls) and assessed for association with CD clinical characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_assertion evidence source_evidence_literature NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_assertion SIO_000772 22573572 NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_assertion wasDerivedFrom befree-20140225 NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_assertion wasGeneratedBy ECO_0000203 NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP278377.RAJHbb9VR2rcd1EhJwLvQvERdVqWEaG5bmMfSJ_daRhsg130_provenance.