Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_assertion> ?p ?o ?g. }
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- NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_assertion type Assertion NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_head.
- NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_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." NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_provenance.
- NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_assertion evidence source_evidence_literature NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_provenance.
- NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_assertion SIO_000772 16246171 NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_provenance.
- NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_assertion wasDerivedFrom befree-20150227 NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_provenance.
- NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_assertion wasGeneratedBy ECO_0000203 NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_provenance.