Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_assertion type Assertion NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_head.
- NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_assertion description "[Four patients had a deletion of a known movement disorder gene including paroxysmal kinesigenic dyskinesia (PRRT2; n=2), SGCE (myoclonus dystonia, n=1), and TITF1 (benign hereditary chorea, n=1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_provenance.
- NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_assertion evidence source_evidence_literature NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_provenance.
- NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_assertion SIO_000772 22515636 NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_provenance.
- NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_assertion wasDerivedFrom befree-20140225 NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_provenance.
- NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_assertion wasGeneratedBy ECO_0000203 NP824514.RACxvAv2EOgV_-UcfNXINfLiIYiQDqTeZLqSbLH0M9KUI130_provenance.