Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion> ?p ?o ?g. }
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- NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion type Assertion NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_head.
- NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_provenance.
- NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion evidence source_evidence_literature NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_provenance.
- NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion SIO_000772 18028407 NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_provenance.
- NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion wasDerivedFrom lhgdn-20090331 NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_provenance.
- NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion wasGeneratedBy ECO_0000203 NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_provenance.