Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_assertion description "[The autosomal-dominant axonal peripheral neuropathies comprise a genetically heterogeneous group of disorders that are clinically subsumed under Charcot-Marie-Tooth disease type 2 (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_assertion evidence source_evidence_literature NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_assertion SIO_000772 16775367 NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_assertion wasDerivedFrom befree-20140225 NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_assertion wasGeneratedBy ECO_0000203 NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP886469.RA_nrsag8PAEaz-0L0jIS3Sqe6tGs6GLHvAO0cJ1clqGA130_provenance.