Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_assertion description "[Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_assertion evidence source_evidence_literature NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_assertion SIO_000772 10762541 NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_assertion wasDerivedFrom befree-20140225 NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_assertion wasGeneratedBy ECO_0000203 NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939847.RAvtdl-kyZZaS0GGS8vXtmnhYAxQq0VZu9NBc8NBI3yks130_provenance.