Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_assertion description "[Mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) are the most commonly identified cause of Charcot-Marie-Tooth type 2 (CMT2), a dominantly inherited disease characterized by degeneration of peripheral sensory and motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_assertion evidence source_evidence_literature NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_assertion SIO_000772 17215403 NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_assertion wasDerivedFrom befree-20140225 NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_assertion wasGeneratedBy ECO_0000203 NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP383954.RAVVVZmVFqgq5G_J8iVZB1fwk0J9APoV3ycKy2Pjh9nMw130_provenance.