Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_assertion> ?p ?o ?g. }
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- NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_assertion type Assertion NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_head.
- NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_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." NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.
- NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_assertion evidence source_evidence_literature NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.
- NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_assertion SIO_000772 23447592 NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.
- NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_assertion wasDerivedFrom befree-2016 NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.
- NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_assertion wasGeneratedBy ECO_0000203 NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.