Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_assertion> ?p ?o ?g. }
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- NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_assertion type Assertion NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_head.
- NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_assertion wasGeneratedBy ECO_0000218 NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_provenance.
- NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_assertion wasDerivedFrom uniprot-20130724 NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_provenance.
- NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_assertion SIO_000772 15863660 NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_provenance.
- NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_assertion evidence source_evidence_curated NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_provenance.
- NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_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." NP1478.RA1bY5wwsHzo8wJacRUIv0kW3IjUGc-Xzc9c0Dcmn4IN4130_provenance.