Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_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." NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_assertion evidence source_evidence_literature NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_assertion SIO_000772 16246171 NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_assertion wasDerivedFrom befree-2016 NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_assertion wasGeneratedBy ECO_0000203 NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
- befree-2016 importedOn "2016-02-19" NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.