Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_assertion description "[Although ubiquitously expressed, DNM2 was found mutated in two genetic disorders affecting different tissues: autosomal dominant centronuclear myopathy (ADCNM; skeletal muscle) and peripheral Charcot-Marie-Tooth neuropathy (peripheral nerve).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_assertion evidence source_evidence_literature NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_assertion SIO_000772 21514436 NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_assertion wasDerivedFrom befree-2016 NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_assertion wasGeneratedBy ECO_0000203 NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.
- befree-2016 importedOn "2016-02-19" NP889144.RAJQNgoCQe4sLKRxq3mmqs6GSDMWU5Gfbq3bGRkX3nWM8130_provenance.