Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion> ?p ?o ?g. }
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- NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion type Assertion NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_head.
- NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_provenance.
- NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion evidence source_evidence_literature NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_provenance.
- NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion SIO_000772 12402271 NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_provenance.
- NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion wasDerivedFrom befree-2016 NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_provenance.
- NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_assertion wasGeneratedBy ECO_0000203 NP372540.RAqCssnEqs6azb2GuQpvlCWWeHw6xPHC7-J5JBbeH_As0130_provenance.