Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_assertion description "[The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_assertion evidence source_evidence_literature NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_assertion SIO_000772 22877996 NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_assertion wasDerivedFrom befree-20150227 NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_assertion wasGeneratedBy ECO_0000203 NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_provenance.