Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_assertion> ?p ?o ?g. }
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- NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_assertion type Assertion NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_head.
- NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_assertion description "[There was a significantly higher frequency of coinheritance of the hereditary hemochromatosis (HH) HFE mutant allele C282Y in 18 unrelated XLSA hemizygotes than found in the normal population, indicating a role for coinheritance of HFE alleles in the expression of this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_provenance.
- NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_assertion evidence source_evidence_literature NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_provenance.
- NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_assertion SIO_000772 10029606 NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_provenance.
- NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_assertion wasDerivedFrom befree-20150227 NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_provenance.
- NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_assertion wasGeneratedBy ECO_0000203 NP447073.RAJpQeWfy2QeGlXmz_iNTS17KDjGLUFRb2-gimuY5Q99A130_provenance.