Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_assertion evidence source_evidence_literature NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_assertion SIO_000772 10749987 NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_assertion wasDerivedFrom befree-2016 NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_assertion wasGeneratedBy ECO_0000203 NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.
- befree-2016 importedOn "2016-02-19" NP280131.RA9IYCsyeY92iR3N9FXtPrWBVULhFcze3-eTCm8EpfqPs130_provenance.