Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion> ?p ?o ?g. }
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- NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion type Assertion NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_head.
- NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_provenance.
- NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion evidence source_evidence_literature NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_provenance.
- NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion SIO_000772 22243967 NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_provenance.
- NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion wasDerivedFrom befree-20140225 NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_provenance.
- NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion wasGeneratedBy ECO_0000203 NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_provenance.