Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_assertion> ?p ?o ?g. }
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- NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_assertion type Assertion NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_head.
- NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_assertion description "[Angelman syndrome (AS) is a severe disorder of postnatal brain development caused by neuron-specific loss of the HECT (homologous to E6AP carboxy terminus) domain E3 ubiquitin ligase Ube3a/E6AP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_provenance.
- NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_assertion evidence source_evidence_literature NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_provenance.
- NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_assertion SIO_000772 23447592 NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_provenance.
- NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_assertion wasDerivedFrom befree-20150227 NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_provenance.
- NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_assertion wasGeneratedBy ECO_0000203 NP976891.RAi3AAVZBAFgCPJhKF2qQlTHoL7SCHgMNCWsrWqddOnis130_provenance.