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- NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_assertion type Assertion NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_head.
- NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_assertion description "[Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.
- NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_assertion evidence source_evidence_literature NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.
- NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_assertion SIO_000772 14607793 NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.
- NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_assertion wasDerivedFrom befree-2016 NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.
- NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_assertion wasGeneratedBy ECO_0000203 NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.