Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_assertion description "[It was recently discovered that many of the underlying mutations responsible for the familial form of WPW syndrome are located in the gene encoding for the regulatory gamma(2)-subunit (PRKAG2) of the AMP-activated protein kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_assertion evidence source_evidence_literature NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_assertion SIO_000772 16686673 NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_assertion wasDerivedFrom befree-20140225 NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_assertion wasGeneratedBy ECO_0000203 NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP687546.RAQFLc9IO5875Xmu0-GfX_qLzPzUa-yMEhrA563r2KmUY130_provenance.