Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_assertion> ?p ?o ?g. }
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- NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_assertion type Assertion NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_head.
- NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_assertion description "[A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_provenance.
- NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_assertion evidence source_evidence_curated NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_provenance.
- NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_assertion SIO_000772 25401298 NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_provenance.
- NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_assertion wasDerivedFrom ctd_human-2016 NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_provenance.
- NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_assertion wasGeneratedBy ECO_0000218 NP34989.RAGo68hhE19-wMa5PG2mdLtep3pPtVtqH-m8ipR79bOkw130_provenance.