Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_assertion description "[A point mutation or a small deletion of mitochondrial DNA, probably affecting the COX-II gene, may be responsible for the COX deficiency in this case of MERRF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_assertion evidence source_evidence_literature NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_assertion SIO_000772 2549843 NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_assertion wasDerivedFrom befree-2016 NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_assertion wasGeneratedBy ECO_0000203 NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247083.RAei51zfOMewtSWLRh4f_mKAA_K-rk9k6WjJfzVt8Pca0130_provenance.