Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_assertion description "[We will also describe the finding of a novel polymorphism in the EAAT2 promoter region which could be responsible for differences in both gene function and regulation under pathological conditions such as cerebral ischemia, and which might well account for the failure of glutamate antagonists in the clinical practice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_assertion evidence source_evidence_literature NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_assertion SIO_000772 16651809 NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_assertion wasDerivedFrom befree-20150227 NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_assertion wasGeneratedBy ECO_0000203 NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP695294.RAEFbFtsSf36mYMknAJF9Dkppmz6EIHvPVByfcKRnQQeg130_provenance.