Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_assertion description "[Homozygosity mapping of 5 patients from a consanguineous family with infantile mitochondrial encephalomyopathy resulted in the identification of a missense mutation in a conserved residue of the C6ORF66.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_assertion evidence source_evidence_literature NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_assertion SIO_000772 18179882 NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_assertion wasDerivedFrom lhgdn-20090331 NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_assertion wasGeneratedBy ECO_0000203 NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209830.RA2ytlA-hkR4gdg9Mm_AKILocRHNYaevvLqKTh8y8OsdY130_provenance.