Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- 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." provenance.
- 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.
- NP823962.RA3t6n8ZMQkL2uZReU5gqaJoFpERr_kjJP3ZiR5vQpsFA130_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." NP823962.RA3t6n8ZMQkL2uZReU5gqaJoFpERr_kjJP3ZiR5vQpsFA130_provenance.