Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_assertion> ?p ?o ?g. }
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- NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_assertion type Assertion NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_head.
- NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_assertion description "[In addition to new mutations in known SCD genes, several novel genes not previously implicated in SCD causation have been found, particularly in long QT syndrome (e.g., KCNJ5, AKAP9, SNTA1), idiopathic ventricular fibrillation (e.g., DPP6, KCNJ8), dilated cardiomyopathy (e.g., NEBL), and hypertrophic cardiomyopathy (HCM; e.g., NEXN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_provenance.
- NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_assertion evidence source_evidence_literature NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_provenance.
- NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_assertion SIO_000772 21430528 NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_provenance.
- NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_assertion wasDerivedFrom befree-20150227 NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_provenance.
- NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_assertion wasGeneratedBy ECO_0000203 NP522447.RAKqYyofGdk44X9nd5g1ZIrMxWdwkP_A2ehCt8w5FKEXM130_provenance.