Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_assertion description "[Targeted mutational analysis of exon 18 in SCN5A of the African-American SIDS cohort (n = 71) revealed the S1103Y polymorphism in 16 (22.5%) of 71 African-American cases of SIDS compared to 135 (11.6%) of 1,161 ostensibly healthy adult African Americans (P = .01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_assertion evidence source_evidence_literature NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_assertion SIO_000772 18452875 NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_assertion wasDerivedFrom befree-20140225 NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_assertion wasGeneratedBy ECO_0000203 NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP291438.RA6fkjXMsWxeYCuE6O0UIW9J4MuP2OkSvbFYzmK3Y_1uI130_provenance.