Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_assertion description "[A novel mutation of the MFN2 gene in a Chinese family with Charcot-Marie-Tooth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_assertion evidence source_evidence_literature NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_assertion SIO_000772 22653593 NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_assertion wasDerivedFrom befree-2016 NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_assertion wasGeneratedBy ECO_0000203 NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.
- befree-2016 importedOn "2016-02-19" NP986381.RAXYndnX5fvM56PkV60UhiKtuQXC83ViviCIZLEzdiLXg130_provenance.