Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_assertion evidence source_evidence_literature NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_assertion SIO_000772 17467628 NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_assertion wasDerivedFrom befree-20150227 NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_assertion wasGeneratedBy ECO_0000203 NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.