Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1056589.RAWyobR-XzAEgaSBJhsTjFmjn9FqDB_1KtSPpQJNJ-z0I130_provenance.