Matches in Nanopublications for { ?s ?p "[Hemochromatosis is a recessively inherited disorder caused by a point mutation, C282Y of the HFE gene on chromosome 6p21.3 near the human leukocyte antigen (HLA) locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_assertion description "[Hemochromatosis is a recessively inherited disorder caused by a point mutation, C282Y of the HFE gene on chromosome 6p21.3 near the human leukocyte antigen (HLA) locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363489.RA-30s9ZD01eWwzNgPXSnzLWGKu1In9iXQcYJPVq5co-A130_provenance.