Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_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." NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_assertion evidence source_evidence_literature NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_assertion SIO_000772 16047349 NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_assertion wasDerivedFrom befree-20140225 NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_assertion wasGeneratedBy ECO_0000203 NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP530302.RAQaXQEAbMCGRg2b1ID5T6WOuTy5-_F69wWM6zEYMemwQ130_provenance.