Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_assertion wasGeneratedBy ECO_0000203 NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_assertion wasDerivedFrom befree-20150227 NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_assertion SIO_000772 23065794 NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_assertion evidence source_evidence_literature NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.
- NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_assertion description "[Nerve excitability studies were performed on eight adults with KCNQ2 mutations and a history of benign familial neonatal epilepsy, now in remission.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523357.RAjtFi0_F6rDO5LpyiA0wKyyMasWqVlzUP6P1sQzu6WC8130_provenance.