Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_assertion description "[Only 5 SCN5A mutations have been associated with LQTS, and more work is needed to improve correlations between SCN5A genotypes and associated clinical syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_assertion evidence source_evidence_literature NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_assertion SIO_000772 10377081 NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_assertion wasDerivedFrom befree-2016 NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_assertion wasGeneratedBy ECO_0000203 NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.
- befree-2016 importedOn "2016-02-19" NP255605.RAsqGoQzWEiRc9cyD1Nks3EalG_eebd4FpjRHiZnaOVwM130_provenance.