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- source_evidence_literature type ECO_0000212 NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_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." NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_assertion evidence source_evidence_literature NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_assertion SIO_000772 18752142 NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_assertion wasDerivedFrom gad-20150221 NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_assertion wasGeneratedBy ECO_0000203 NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129137.RAO9Tc1M30wBtUdaFoQVR2bHdHoSxsgz5ezs3Jw7KghSE130_provenance.