Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_assertion description "[We here present a detailed functional analysis of Na(v)1.2 mutant, R1312T, which was originally found in a child with Dravet syndrome (formerly known as severe myoclonic epilepsy of infancy or SMEI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_assertion evidence source_evidence_literature NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_assertion SIO_000772 22677033 NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_assertion wasDerivedFrom befree-2016 NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_assertion wasGeneratedBy ECO_0000203 NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.
- befree-2016 importedOn "2016-02-19" NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.