Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion evidence source_evidence_literature NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion SIO_000772 11739564 NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion wasDerivedFrom befree-2016 NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion wasGeneratedBy ECO_0000203 NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- befree-2016 importedOn "2016-02-19" NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.