Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_assertion> ?p ?o ?g. }
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- NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_assertion type Assertion NP354354.RA3aAhaeNuUbJ7HPVw1Z5iSA8dstEOpVgO8E5UaTIVdpE130_head.
- 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.