Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion type Assertion NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_head.
- NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion description "[Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_provenance.
- NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion evidence source_evidence_literature NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_provenance.
- NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion SIO_000772 11468227 NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_provenance.
- NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion wasDerivedFrom befree-2016 NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_provenance.
- NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion wasGeneratedBy ECO_0000203 NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_provenance.