Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_assertion evidence source_evidence_literature NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_assertion SIO_000772 23631824 NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_assertion wasDerivedFrom befree-20140225 NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_assertion wasGeneratedBy ECO_0000203 NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.