Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_assertion description "[H558R polymorphism in SCN5A is associated with Keshan disease and QRS prolongation in Keshan disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_assertion evidence source_evidence_literature NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_assertion SIO_000772 25177937 NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_assertion wasDerivedFrom befree-2016 NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_assertion wasGeneratedBy ECO_0000203 NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215907.RASeef2SJHmfL1cbPf_0ocl8t0TJ3ZHpqf6jl8nsM-gRc130_provenance.