Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_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." NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_assertion evidence source_evidence_literature NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_assertion SIO_000772 16686673 NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_assertion wasDerivedFrom befree-2016 NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_assertion wasGeneratedBy ECO_0000203 NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.
- befree-2016 importedOn "2016-02-19" NP549058.RAjq5eLXo-F_Ri8hdgie__MXB4o1ssg6gFRZkKHztnIhU130_provenance.