Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_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." NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_assertion evidence source_evidence_literature NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_assertion SIO_000772 14607793 NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_assertion wasDerivedFrom gad-20150221 NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_assertion wasGeneratedBy ECO_0000203 NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69684.RAWDFhUJxHAZS7ntSTUsc-T0vZ6YMC_GcBfGfs0bE7CeM130_provenance.