Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_assertion> ?p ?o ?g. }
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- NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_assertion type Assertion NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_head.
- NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_assertion description "[Mutations in the DNM2 gene cause two hereditary neuromuscular disorders: dominant centronuclear myopathy and Charcot-Marie-Tooth peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_provenance.
- NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_assertion evidence source_evidence_literature NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_provenance.
- NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_assertion SIO_000772 23609221 NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_provenance.
- NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_assertion wasDerivedFrom befree-2016 NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_provenance.
- NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_assertion wasGeneratedBy ECO_0000203 NP1071539.RAVQyGVV-eXmsOgEFA4artvTK_y1tLQg_pP7lz7VBhLqQ130_provenance.