Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP419947.RAe9-ulv02kVgbngN8sbnkl0_HIqW75jujHEVbRYq1dRs130_provenance.