Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_assertion> ?p ?o ?g. }
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- NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_assertion type Assertion NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_head.
- 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.
- NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_assertion evidence source_evidence_curated NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_provenance.
- NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_assertion SIO_000772 17469202 NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_provenance.
- NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_assertion wasDerivedFrom ctd_human-20130708 NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_provenance.
- NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_assertion wasGeneratedBy ECO_0000218 NP21717.RAJWNtDrGLAHPjgIkrW0ermF8lIM1d8WK7Uy6-4jrodWY130_provenance.