Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_assertion description "[Although all previously reported mutations in the SURF1 gene have been found in patients with cytochrome oxidase (COX)-deficient Leigh syndrome, the phenotype associated with SURF1 protein deficiency should be extended to include leukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_assertion evidence source_evidence_literature NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_assertion SIO_000772 11409433 NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_assertion wasDerivedFrom befree-20140225 NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_assertion wasGeneratedBy ECO_0000203 NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP235356.RAe-eW9DNnEH0Qn6XiNEnPdC6-7XAGLHT7DIcvSdMixZQ130_provenance.