Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_assertion> ?p ?o ?g. }
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- NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_assertion type Assertion NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_head.
- NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_assertion wasGeneratedBy ECO_0000203 NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_provenance.
- NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_assertion wasDerivedFrom befree-20140225 NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_provenance.
- NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_assertion SIO_000772 22606975 NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_provenance.
- NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_assertion evidence source_evidence_literature NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_provenance.
- NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_assertion description "[Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842402.RAcnYxBNG4Tb56upz2MK5r3OgH3D1o85P6-LDqUcFhKOM130_provenance.