Matches in Nanopublications for { ?s ?p "[Hutchinson-Gilford progeria syndrome (HGPS) is a rare precocious aging syndrome caused by mutations in LMNA that lead to synthesis of a mutant form of prelamin A, generally called progerin, that cannot be processed to mature lamin A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_assertion description "[Hutchinson-Gilford progeria syndrome (HGPS) is a rare precocious aging syndrome caused by mutations in LMNA that lead to synthesis of a mutant form of prelamin A, generally called progerin, that cannot be processed to mature lamin A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_provenance.
- assertion description "[Hutchinson-Gilford progeria syndrome (HGPS) is a rare precocious aging syndrome caused by mutations in LMNA that lead to synthesis of a mutant form of prelamin A, generally called progerin, that cannot be processed to mature lamin A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_assertion description "[Hutchinson-Gilford progeria syndrome (HGPS) is a rare precocious aging syndrome caused by mutations in LMNA that lead to synthesis of a mutant form of prelamin A, generally called progerin, that cannot be processed to mature lamin A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_provenance.