Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_assertion> ?p ?o ?g. }
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- NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_assertion type Assertion NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_head.
- NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_assertion description "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature-aging syndrome caused by a dominant mutation in the gene encoding lamin A, which leads to an aberrantly spliced and processed protein termed progerin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_provenance.
- NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_assertion evidence source_evidence_literature NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_provenance.
- NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_assertion SIO_000772 20605919 NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_provenance.
- NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_assertion wasDerivedFrom befree-2016 NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_provenance.
- NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_assertion wasGeneratedBy ECO_0000203 NP823960.RAcCCHHVvy9f7G630VJru9_fYnO1Pzr3-lqezSwfm3JuQ130_provenance.