Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_assertion description "[The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_assertion evidence source_evidence_literature NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_assertion SIO_000772 17412732 NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_assertion wasDerivedFrom befree-20140225 NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_assertion wasGeneratedBy ECO_0000203 NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_provenance.