Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_assertion> ?p ?o ?g. }
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- NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_assertion type Assertion NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_head.
- NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_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." NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.
- NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_assertion evidence source_evidence_literature NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.
- NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_assertion SIO_000772 23447592 NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.
- NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_assertion wasDerivedFrom befree-20140225 NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.
- NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_assertion wasGeneratedBy ECO_0000203 NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.