Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP810596.RASBCTKY4voIHsVM6R6tSZH4-THFNsmH7hk6SQn8-J0UY130_provenance.