Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_assertion description "[Specifically, carriage of the ADRA2B deletion abolished the relative memory impairment in homozygous COMT val(158) carriers compared to met(158) carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_assertion evidence source_evidence_literature NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_assertion SIO_000772 20110158 NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_assertion wasDerivedFrom befree-20150227 NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_assertion wasGeneratedBy ECO_0000203 NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP226535.RABH_3Th9bMILF9Zmi6fltKf7nuaS8as2kbh6gnHklNLE130_provenance.