Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_assertion description "[We report in an affected man and his mother an adult-onset form of childhood ataxia with central nervous system hypomyelination/vanishing white matter disease-like disorder with no mutations in the EIF2B genes and normal guanine nucleotide exchange factor eIF2B activity, suggesting a new dominant inheritance of this syndrome that may involve other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_assertion evidence source_evidence_literature NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_assertion SIO_000772 16047349 NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_assertion wasDerivedFrom befree-20140225 NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_assertion wasGeneratedBy ECO_0000203 NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP426777.RABhCJhF4WJjnPb8jDo-IU3K4hGhvAPQAaJgclB_tR7AQ130_provenance.