Matches in Nanopublications for { ?s ?p "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504179.RAn_YUe7gZqQkY14ZpU6Ar3lj8SMOmVDjG9kah327Ny4E130_provenance.
- NP663753.RAvT2OCNVL8ybpzA0vDlTS4J9BL_rAg8azk_vJDNsI9ag130_assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663753.RAvT2OCNVL8ybpzA0vDlTS4J9BL_rAg8azk_vJDNsI9ag130_provenance.
- NP354981.RAJ911i0a10TdQJTrEZoXsFPHzW5JgVV0k4SYKzNG7opA130_assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354981.RAJ911i0a10TdQJTrEZoXsFPHzW5JgVV0k4SYKzNG7opA130_provenance.
- NP615988.RA5l4I2XhtjOT37-BwmtFMoaMK-HXubyLVh2e0Kme0xGo130_assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615988.RA5l4I2XhtjOT37-BwmtFMoaMK-HXubyLVh2e0Kme0xGo130_provenance.
- assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP990504.RASjtQHoGa-vs8Yyl5eCxjk3SO1DVaq2ChdI0tOkvhC84130_assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990504.RASjtQHoGa-vs8Yyl5eCxjk3SO1DVaq2ChdI0tOkvhC84130_provenance.
- NP990500.RA0qHRy7IuZW9VcPWuN7WFj3FQAfGKD1LQ3W3aEJC1RAA130_assertion description "[Childhood SMA associated with progressive myoclonic epilepsy (SMA-PME) has been reported as a rare autosomal-recessive condition unlinked to mutations in SMN1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990500.RA0qHRy7IuZW9VcPWuN7WFj3FQAfGKD1LQ3W3aEJC1RAA130_provenance.