Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_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." NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_assertion evidence source_evidence_literature NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_assertion SIO_000772 22515636 NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_assertion wasDerivedFrom befree-2016 NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_assertion wasGeneratedBy ECO_0000203 NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.
- befree-2016 importedOn "2016-02-19" NP976013.RArj1byXkdZ5DS8V7suCvBZ4gLCjeJER5QOs_bJPSkOIM130_provenance.