Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_assertion description "[Hemochromatosis is considered by many to be an uncommon disorder, although the prevalence of HFE (High Iron) 282 Cys ? Tyr (C282Y) homozygosity is relatively high in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_assertion evidence source_evidence_literature NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_assertion SIO_000772 22183642 NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_assertion wasDerivedFrom befree-2016 NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_assertion wasGeneratedBy ECO_0000203 NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.
- befree-2016 importedOn "2016-02-19" NP947948.RAf4hExJvRANJCmkiZoJndQg0eUJ2vtk6Fp7R4G_UwSXM130_provenance.