Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_assertion description "[Because KVLQT1 mutations cause arrhythmia susceptibility in the long QT syndrome (LQT), we hypothesized that mutations in KCNE1 also cause this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_assertion evidence source_evidence_literature NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_assertion SIO_000772 9354802 NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_assertion wasDerivedFrom befree-20140225 NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_assertion wasGeneratedBy ECO_0000203 NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380806.RAG0s_LE3HhXs0qHiOkuygHSuXSbHd0uPqL04u4zmnmS8130_provenance.