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- source_evidence_literature type ECO_0000212 NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_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." NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_assertion evidence source_evidence_literature NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_assertion SIO_000772 23447592 NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_assertion wasDerivedFrom befree-20150227 NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_assertion wasGeneratedBy ECO_0000203 NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP608765.RAr5_Fkdr6EUviyB7xiH70Yo9NalbrBjX1YS8lfHcdIDE130_provenance.