Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_assertion type Assertion NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_head.
- NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_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." NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_provenance.
- NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_assertion evidence source_evidence_literature NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_provenance.
- NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_assertion SIO_000772 21430528 NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_provenance.
- NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_assertion wasDerivedFrom befree-20150227 NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_provenance.
- NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_assertion wasGeneratedBy ECO_0000203 NP522513.RAW6r7ozWE2p-KQrcF4HpOqKXs0Df_TXu3B6YECwE49mg130_provenance.