Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_assertion wasGeneratedBy ECO_0000203 NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_assertion wasDerivedFrom befree-20150227 NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_assertion SIO_000772 9541114 NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_assertion evidence source_evidence_literature NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.
- NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.