Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_assertion evidence source_evidence_literature NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_assertion SIO_000772 16246171 NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_assertion wasDerivedFrom befree-20150227 NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_assertion wasGeneratedBy ECO_0000203 NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.