Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion type Assertion NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_head.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion evidence source_evidence_literature NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion SIO_000772 22926851 NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion wasDerivedFrom befree-20150227 NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion wasGeneratedBy ECO_0000203 NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.