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- NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_assertion type Assertion NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_head.
- NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_assertion description "[Mutations in the eukaryotic translation initiation factor 2B (eIF2B) represent a heterogenous group of autosomal recessive leucodystrophy characterized by a diffuse CSF-like aspect of the white matter at MRI designed as vanishing white matter (VWM) and episodes of acute deterioration after stresses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_provenance.
- NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_assertion evidence source_evidence_literature NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_provenance.
- NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_assertion SIO_000772 18005052 NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_provenance.
- NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_assertion wasDerivedFrom befree-20150227 NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_provenance.
- NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_assertion wasGeneratedBy ECO_0000203 NP810451.RAIkTKMwhwC01T4axpW6xcBrILnss3_0yHxNRif9w25AQ130_provenance.