Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP963736.RAEUhKxnAGf9kyVBfDNjxvwVDH_XBk8d36EcnsgIypSaQ130_provenance.