Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_assertion> ?p ?o ?g. }
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- NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_assertion type Assertion NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_head.
- NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_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." NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_provenance.
- NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_assertion evidence source_evidence_literature NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_provenance.
- NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_assertion SIO_000772 18028407 NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_provenance.
- NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_assertion wasDerivedFrom lhgdn-20090331 NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_provenance.
- NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_assertion wasGeneratedBy ECO_0000203 NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_provenance.