Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_assertion> ?p ?o ?g. }
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- NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_assertion type Assertion NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_head.
- NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_assertion description "[These results indicate that, except for SCN5A, rare coding variation in previously reported arrhythmia-susceptibility genes do not contribute significantly to the occurrence of BrS in a population with European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_provenance.
- NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_assertion evidence source_evidence_literature NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_provenance.
- NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_assertion SIO_000772 25650408 NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_provenance.
- NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_assertion wasDerivedFrom befree-2016 NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_provenance.
- NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_assertion wasGeneratedBy ECO_0000203 NP1260902.RA5MNX3BvrKJlrgC93lS1STfqjOFuhjqLrlH0KuHrfa1k130_provenance.