Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion type Assertion NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_head.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_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." NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion evidence source_evidence_literature NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion SIO_000772 20605919 NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion wasDerivedFrom befree-20140225 NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.
- NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_assertion wasGeneratedBy ECO_0000203 NP445222.RA1iKuyZVmPqEaaGEa5LLiDUFaat1bgYJnnDIetxVTpyk130_provenance.