Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_assertion description "[Both MYO9B rs7259292 and HLA-DQ2 homozygosity increase the risk for RCD II and EATL to a similar extent when compared with uncomplicated CD patients (OR, 4.3; 95% CI, 1.9-9.8 and OR, 5.4; 95% CI, 3.0-9.6, respectively), but there was no evidence for any interaction between these 2 risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_assertion evidence source_evidence_literature NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_assertion SIO_000772 17967566 NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_assertion wasDerivedFrom befree-20140225 NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_assertion wasGeneratedBy ECO_0000203 NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651034.RArx8dJ1Ve-ARn9PT2YG4RcdGp4il7E_O1NkeWqVeoeZE130_provenance.