Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_assertion description "[We report the first case of leukodystrophy with systemic cytochrome oxidase deficiency caused by a loss of function mutation in the SURF1 gene in a 2-year-old girl presenting with failure to thrive, global neurodevelopmental regression, and lactic acidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_assertion evidence source_evidence_literature NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_assertion SIO_000772 11409433 NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_assertion wasDerivedFrom befree-20140225 NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_assertion wasGeneratedBy ECO_0000203 NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP185870.RAuSvK2CPinIFgLXEN_J7j9skOjcFnZmNbrbGiNAZYlYw130_provenance.