Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_assertion description "[, 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." NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_assertion evidence source_evidence_literature NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_assertion SIO_000772 18079478 NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_assertion wasDerivedFrom gad-20150221 NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_assertion wasGeneratedBy ECO_0000203 NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP106197.RAYVwYCsx4UiMULV0bZ2NmiuXHt6EO5uc9H537o7bIKGI130_provenance.