Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- befree-2016 importedOn "2016-02-19" NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_assertion wasGeneratedBy ECO_0000203 NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_assertion wasDerivedFrom befree-2016 NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_assertion SIO_000772 14998624 NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_assertion evidence source_evidence_literature NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.
- NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_assertion description "[Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434009.RAg0BIYymn0ogAIH_v1LzLI9J6r1_02yOAdWbbhmcMutE130_provenance.