Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_assertion> ?p ?o ?g. }
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- NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_assertion type Assertion NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_head.
- NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_assertion wasGeneratedBy ECO_0000203 NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_provenance.
- NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_assertion wasDerivedFrom befree-20140225 NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_provenance.
- NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_assertion SIO_000772 18678442 NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_provenance.
- NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_assertion evidence source_evidence_literature NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_provenance.
- NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_assertion description "[Some of the patients have a variant of `vanishing white matter disease` with mutations in subunits of eukaryotic initiation factor 2B (EIF2B).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP170181.RAezAVu_dGH3d76a6xYpNEU5VuddRyKQy1ZYRYOym2ylQ130_provenance.