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- NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_assertion type Assertion NP963651.RAF41_Npx1Q7n3kFad6GsUSKMy2v1VIvqj_KpiWw44dDM130_head.
- 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.