Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_assertion type Assertion NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_head.
- 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.
- NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_assertion evidence source_evidence_literature NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_provenance.
- NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_assertion SIO_000772 17469202 NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_provenance.
- NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_assertion wasDerivedFrom befree-2016 NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_provenance.
- NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_assertion wasGeneratedBy ECO_0000203 NP607457.RAR--aVJczHHuJYeYKM7xJXp5-W7IevugtB3ZA2I-9hpg130_provenance.