Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_assertion type Assertion NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_head.
- NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_assertion wasGeneratedBy ECO_0000218 NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_provenance.
- NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_assertion wasDerivedFrom ctd_human-20150221 NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_provenance.
- NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_assertion SIO_000772 25401298 NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_provenance.
- NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_assertion evidence source_evidence_curated NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_provenance.
- NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_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." NP6085.RAevUsDbZIYNdUe0trQ2vWq03jHT9ACm-625_lWeFqWFc130_provenance.