Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_assertion description "[In summary, in this study we demonstrate for the first time the association of A419C polymorphism of the glyoxalase I gene with sRAGE levels and show the genetic predisposition to vascular complications in HD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_assertion evidence source_evidence_literature NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_assertion SIO_000772 18079478 NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_assertion wasDerivedFrom befree-20150227 NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_assertion wasGeneratedBy ECO_0000203 NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP428710.RAkcLJWrb0oNG4ghK0SrwM5sSkUxhGPzIt5E8wgfqPYbE130_provenance.