Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_assertion> ?p ?o ?g. }
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- NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_assertion type Assertion NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_head.
- NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_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." NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_provenance.
- NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_assertion evidence source_evidence_literature NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_provenance.
- NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_assertion SIO_000772 22515636 NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_provenance.
- NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_assertion wasDerivedFrom befree-2016 NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_provenance.
- NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_assertion wasGeneratedBy ECO_0000203 NP976019.RA_EmUMpDmsHZ57xPTE2H5Q0bPUGHmVOrcsEgfSkcArmg130_provenance.