Matches in Nanopublications for { ?s ?p "[A hypermorphic missense mutation in PLCG2, encoding phospholipase CI32, causes a dominantly inherited autoinflammatory disease with immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1766.RAlrHsBse44SbVhVA3zZVn4QkLvFPsCS-cqu3vuaOsY0s130_assertion description "[A hypermorphic missense mutation in PLCG2, encoding phospholipase CI32, causes a dominantly inherited autoinflammatory disease with immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1766.RAlrHsBse44SbVhVA3zZVn4QkLvFPsCS-cqu3vuaOsY0s130_provenance.