Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_assertion type Assertion NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_head.
- NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_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." NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_provenance.
- NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_assertion evidence source_evidence_literature NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_provenance.
- NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_assertion SIO_000772 16686673 NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_provenance.
- NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_assertion wasDerivedFrom befree-2016 NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_provenance.
- NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_assertion wasGeneratedBy ECO_0000203 NP549056.RAu5banDcnmWb4MnSv8DdPv67IPMRuG5kzFUby8Y8ojhk130_provenance.