Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_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." NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_assertion evidence source_evidence_literature NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_assertion SIO_000772 18812404 NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_assertion wasDerivedFrom befree-2016 NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_assertion wasGeneratedBy ECO_0000203 NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.
- befree-2016 importedOn "2016-02-19" NP694555.RAUnI5gXAhHjtdjcky8yOPQSrwj8Vo3QcEMJSM0wC0xLs130_provenance.