Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_assertion description "[Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_assertion evidence source_evidence_literature NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_assertion SIO_000772 10973849 NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_assertion wasDerivedFrom befree-2016 NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_assertion wasGeneratedBy ECO_0000203 NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP294208.RAhSlOvF1aOFsfG0FD2vjDA1m_UwsmpFrFQGBkpjVx0-Y130_provenance.