Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_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." NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_assertion evidence source_evidence_literature NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_assertion SIO_000772 22515636 NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_assertion wasDerivedFrom befree-20150227 NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_assertion wasGeneratedBy ECO_0000203 NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810992.RAAnw59nuUwmjGwwdQE0cNgXYN89HFW2Nql1hbhs2WKkM130_provenance.