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- NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_assertion type Assertion NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_head.
- NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_assertion wasGeneratedBy ECO_0000203 NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_provenance.
- NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_assertion wasDerivedFrom befree-20140225 NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_provenance.
- NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_assertion SIO_000772 15863660 NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_provenance.
- NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_assertion evidence source_evidence_literature NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_provenance.
- NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_assertion description "[Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502878.RAPimE21KpatSF_ms4W1dzBS-6OLWCKAutDa9hBSpIqt8130_provenance.