Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_assertion type Assertion NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_head.
- NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_assertion wasGeneratedBy ECO_0000203 NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_provenance.
- NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_assertion wasDerivedFrom befree-2016 NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_provenance.
- NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_assertion SIO_000772 25218114 NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_provenance.
- NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_assertion evidence source_evidence_literature NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_provenance.
- NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_assertion description "[The present findings confirm that PCDH19 is a major causative gene for infantile onset familial or sporadic epilepsy in female patients with or without mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1219850.RAbKcA-8Ccn_ai2ceVi6eGsItTksv0SoI741Dj6U7y2kc130_provenance.