Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_assertion description "[The most common mutation of HFE, C282Y, has a Celtic origin and most patients with HH are homozygous for it in Northern European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_assertion evidence source_evidence_literature NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_assertion SIO_000772 12002748 NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_assertion wasDerivedFrom befree-2016 NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_assertion wasGeneratedBy ECO_0000203 NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.
- befree-2016 importedOn "2016-02-19" NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_provenance.