Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_assertion description "[Here, we report that disruption of frabin/FGD4, a GEF for the Rho GTPase cell-division cycle 42 (Cdc42), causes peripheral nerve demyelination in patients with autosomal recessive Charcot-Marie-Tooth (CMT) neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_assertion evidence source_evidence_literature NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_assertion SIO_000772 17564972 NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_assertion wasDerivedFrom befree-20140225 NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_assertion wasGeneratedBy ECO_0000203 NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP497853.RA__rNoGOt0fvhCWGf6YVs796WJ9pNvVurwroa9dplDwI130_provenance.