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- NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_assertion type Assertion NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_head.
- NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_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." NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_provenance.
- NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_assertion evidence source_evidence_literature NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_provenance.
- NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_assertion SIO_000772 22515636 NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_provenance.
- NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_assertion wasDerivedFrom befree-20140225 NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_provenance.
- NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_assertion wasGeneratedBy ECO_0000203 NP826860.RA1N37xXl_OzsQyh0n-sH7jHcoLTVfMqbEJYRwJUXVzHQ130_provenance.