Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_assertion description "[In the present study, specific missense mutations in the mitochondrial CO1 and CO2 genes but not the CO3 gene were found to segregate at a higher frequency with AD compared with other neurodegenerative or metabolic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_assertion evidence source_evidence_literature NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_assertion SIO_000772 9114023 NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_assertion wasDerivedFrom befree-2016 NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_assertion wasGeneratedBy ECO_0000203 NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1371111.RAx64_g7dT1UQJ6yMOGm2dm0CA3X6ORHTl20vyKHDidwo130_provenance.