Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_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." NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_assertion evidence source_evidence_literature NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_assertion SIO_000772 10762541 NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_assertion wasDerivedFrom befree-20140225 NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_assertion wasGeneratedBy ECO_0000203 NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP385721.RA2RL1zfP6tmP448nC4r-BBKCXbE4lLpDrES_Ll3wzTiY130_provenance.