Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_assertion description "[Mutations in PRKAG2 have been described in patients with familial WPW syndrome and hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_assertion evidence source_evidence_literature NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_assertion SIO_000772 18812404 NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_assertion wasDerivedFrom befree-20140225 NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_assertion wasGeneratedBy ECO_0000203 NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP460579.RAZVT9x-HXvYftwnVw1x3ScDpJQ__2QCJlHI_6QU3mMY0130_provenance.