Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_assertion> ?p ?o ?g. }
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- NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_assertion type Assertion NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_head.
- NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_assertion description "[Episodic ataxia type 1 (EA1) is caused by mutations in the KCNA1 gene encoding the fast potassium channel Kv1.1 and is characterized clinically by brief episodes of ataxia and continuous and spontaneous motor unit activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_provenance.
- NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_assertion evidence source_evidence_literature NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_provenance.
- NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_assertion SIO_000772 23909822 NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_provenance.
- NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_assertion wasDerivedFrom befree-20140225 NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_provenance.
- NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_assertion wasGeneratedBy ECO_0000203 NP642382.RABJ5_Tcp_qhLa6XcO2QTovUPRvI4L71v2vXpdNUVLOdk130_provenance.