Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_assertion description "[Recent observations suggest that the human episodic ataxia 2 (EA2) and spinocerebellar ataxia types 6 (SCA6), 12 (SCA12), and 14 (SCA14) might be associated with impaired phosphorylation levels of cerebellum calcium channels and receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_assertion evidence source_evidence_literature NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_assertion SIO_000772 19488825 NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_assertion wasDerivedFrom befree-20140225 NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_assertion wasGeneratedBy ECO_0000203 NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP312856.RA8W0nogMrjEG4A4a9dYF6nH23SuAzKIc8wotmTDcD3X8130_provenance.