Matches in Nanopublications for { ?s ?p "[Hutchinson-Gilford progeria syndrome (HGPS) is a genetic disorder displaying features reminiscent of premature senescence caused by germline mutations in the LMNA gene encoding lamin A and C, essential components of the nuclear lamina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP379658.RAmfmb90IzcY6QeivlU2lTseetGdr9rAv1UMxOzG5M2o8130_assertion description "[Hutchinson-Gilford progeria syndrome (HGPS) is a genetic disorder displaying features reminiscent of premature senescence caused by germline mutations in the LMNA gene encoding lamin A and C, essential components of the nuclear lamina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379658.RAmfmb90IzcY6QeivlU2lTseetGdr9rAv1UMxOzG5M2o8130_provenance.