Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_assertion description "[This region also contains a locus for right ventricular cardiomyopathy (ARVD5) and the cardiac sodium channel gene (SCN5A), mutations that cause isolated progressive cardiac conduction defect (Lenegre syndrome), long-QT syndrome (LQT3), and Brugada syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_assertion evidence source_evidence_literature NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_assertion SIO_000772 15466643 NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_assertion wasDerivedFrom befree-20140225 NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_assertion wasGeneratedBy ECO_0000203 NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP890963.RAQQG0EQFTxefS7uUNgUfRZRDK2Za1wJ9mp87euFk5P8A130_provenance.