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- NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_assertion type Assertion NP651319.RA1ijPvsps9YhPQ7GLeT1Tn5Jf2e7sf9hG6Kr8Fjtv_MU130_head.
- 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.