Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_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." NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_assertion evidence source_evidence_literature NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_assertion SIO_000772 23447592 NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_assertion wasDerivedFrom befree-20150227 NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_assertion wasGeneratedBy ECO_0000203 NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP943997.RAZifJFKulsmw2vP05qIqKZyTSX_lYBuiMsUOowGCrD3Q130_provenance.