Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_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." NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_assertion evidence source_evidence_curated NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_assertion SIO_000772 23872634 NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_assertion wasDerivedFrom ctd_human-2016 NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_assertion wasGeneratedBy ECO_0000218 NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP33237.RAEt_vG5qLkmc_9pFasMq6raLpCiyO8CPdmZAQ5fz1XHU130_provenance.