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- source_evidence_literature type ECO_0000212 NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_assertion description "[Representative of the latter group is Na(v)1.2 (gene name SCN2A): despite its abundance in the brain, Na(v)1.2-related epilepsy is rare and only few studies have been conducted as to the pathophysiological basis of Na(v)1.2 in neuronal hyperexcitability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_assertion evidence source_evidence_literature NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_assertion SIO_000772 22677033 NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_assertion wasDerivedFrom befree-2016 NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_assertion wasGeneratedBy ECO_0000203 NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.
- befree-2016 importedOn "2016-02-19" NP988061.RAj-hPGYHV8alNIW5wouEV9AiCEZNIotMrg0sqSr89O28130_provenance.