Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_assertion> ?p ?o ?g. }
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- NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_assertion type Assertion NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_head.
- NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_assertion wasGeneratedBy ECO_0000203 NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_provenance.
- NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_assertion wasDerivedFrom befree-20140225 NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_provenance.
- NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_assertion SIO_000772 15863660 NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_provenance.
- NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_assertion evidence source_evidence_literature NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_provenance.
- NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_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." NP694869.RAewJGIQ5LOMZfkAh0QWnrNTmx8XKbggQK64DkHI6L_SI130_provenance.