Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_assertion> ?p ?o ?g. }
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- NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_assertion type Assertion NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_head.
- NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_assertion description "[It has recently been discovered that mutations in the genes encoding the five subunits of eukaryocytic initiation factor 2B (eIF2B) are the cause of vanishing white-matter disease/childhood ataxia with central hypomyelination syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.
- NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_assertion evidence source_evidence_literature NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.
- NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_assertion SIO_000772 15021247 NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.
- NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_assertion wasDerivedFrom befree-20150227 NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.
- NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_assertion wasGeneratedBy ECO_0000203 NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.