Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_assertion description "[Mutations in the KCNQ1, HERG, SCN5A, minK and MiRP1 genes cause long QT syndrome (LQTS), of which there are two forms: the Romano Ward syndrome and the Jervell and Lange-Nielsen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_assertion evidence source_evidence_literature NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_assertion SIO_000772 18752142 NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_assertion wasDerivedFrom befree-20140225 NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_assertion wasGeneratedBy ECO_0000203 NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP605577.RAQkKy7MW_BbQ0vsTv8DkiBDVUcoj-VCo7N8HMFdxmWRA130_provenance.