Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_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." NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_assertion evidence source_evidence_literature NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_assertion SIO_000772 17564972 NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_assertion wasDerivedFrom befree-20140225 NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_assertion wasGeneratedBy ECO_0000203 NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP494176.RAC9uueM9kv57hK1l7pi5ZUnPQbuHWsJEHVlSUSm1M9sI130_provenance.