Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_assertion description "[Whereas in hereditary hemochromatosis patients without CD, DMT1 expression was up-regulated leading to excessive uptake of iron, we identified a significant reduction in protein and mRNA expression of DMT1 as a compensatory mechanism in this patient with HH and CD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_assertion evidence source_evidence_literature NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_assertion SIO_000772 15929194 NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_assertion wasDerivedFrom befree-2016 NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_assertion wasGeneratedBy ECO_0000203 NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.
- befree-2016 importedOn "2016-02-19" NP497392.RAvIkCyNSujffRX1Z-cuLUguwf5mKwz096SkLM9dDBGp4130_provenance.