Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_assertion wasGeneratedBy ECO_0000203 NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_assertion wasDerivedFrom gad-20150221 NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_assertion SIO_000772 20851114 NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_assertion evidence source_evidence_literature NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.
- NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_assertion description "[This HRM/sequencing procedure represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent LQTS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186075.RAC1yYAu3Z8F58V3GbE--3cTXNc0NcbMiDySLnxBi31uQ130_provenance.