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- source_evidence_literature type ECO_0000212 NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_assertion description "[However, recently released exome data make some of the prior associations of BrS with genes SCN3B, MOG1, and KCND3 less likely.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_assertion evidence source_evidence_literature NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_assertion SIO_000772 22284586 NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_assertion wasDerivedFrom befree-2016 NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_assertion wasGeneratedBy ECO_0000203 NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.
- befree-2016 importedOn "2016-02-19" NP956549.RAfUKRLGNXImWLjE18iKqsL37aXvkQbkmKCvC3hAzefq0130_provenance.