Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_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." NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_assertion evidence source_evidence_literature NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_assertion SIO_000772 23398397 NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_assertion wasDerivedFrom befree-20140225 NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_assertion wasGeneratedBy ECO_0000203 NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP258207.RA3UwXzTE4Edt41Wg_6iwM4TllLjnGplgamOeAl0Z7-rM130_provenance.