Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP678759.RAD9nHSNZt0-fSeGOnii9X-VuIHNAU2ES5M89wtw6tBtk130_provenance.