Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_assertion> ?p ?o ?g. }
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- NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_assertion type Assertion NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_head.
- NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_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." NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_provenance.
- NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_assertion evidence source_evidence_literature NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_provenance.
- NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_assertion SIO_000772 16686673 NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_provenance.
- NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_assertion wasDerivedFrom befree-20140225 NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_provenance.
- NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_assertion wasGeneratedBy ECO_0000203 NP835025.RAYQd8whKQrd_4lPGxXKx_eK86JOVtJeq8r3WLMkTmxSA130_provenance.