Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_assertion description "[A recent study has revealed that loss of neuronal expression of the paternally imprinted gene Ube3a in Angelman syndrome results in selective neuronal loss of robust circadian oscillations, with a resulting behavioural phenotype, and adipose tissue accumulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_assertion evidence source_evidence_literature NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_assertion SIO_000772 25734270 NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_assertion wasDerivedFrom befree-2016 NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_assertion wasGeneratedBy ECO_0000203 NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267697.RAML8008VxEP3oGzql-_VP-RyUszAhqj3vlqAdtJxQXOo130_provenance.