Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion> ?p ?o ?g. }
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- NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion type Assertion NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_head.
- NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
- NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion evidence source_evidence_literature NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
- NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion SIO_000772 23398397 NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
- NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion wasDerivedFrom befree-20150227 NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
- NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_assertion wasGeneratedBy ECO_0000203 NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.