Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_assertion> ?p ?o ?g. }
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- NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_assertion type Assertion NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_head.
- NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_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." NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_provenance.
- NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_assertion evidence source_evidence_literature NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_provenance.
- NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_assertion SIO_000772 12402271 NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_provenance.
- NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_assertion wasDerivedFrom befree-20140225 NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_provenance.
- NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_assertion wasGeneratedBy ECO_0000203 NP184624.RA69LznUyW80ITQ4TUwYW8g4U8UrgMD5AnWCzZRr4oyfM130_provenance.