Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion wasGeneratedBy ECO_0000203 NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion wasDerivedFrom befree-20150227 NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion SIO_000772 10359058 NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion evidence source_evidence_literature NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion description "[These findings imply a contribution of the UGT1A polymorphism associated to Gilbert's syndrome to development of the hyperbilirubinemia in G6PD deficient subjects during acute hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.