Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_assertion> ?p ?o ?g. }
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- NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_assertion type Assertion NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_head.
- NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_assertion description "[Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_provenance.
- NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_assertion evidence source_evidence_curated NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_provenance.
- NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_assertion SIO_000772 23872634 NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_provenance.
- NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_assertion wasDerivedFrom ctd_human-2016 NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_provenance.
- NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_assertion wasGeneratedBy ECO_0000218 NP33238.RA8eDAOhOEK2hammcvXGQReUa-Wz1ub50m_q4OQJAtJlw130_provenance.