Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_assertion type Assertion NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_head.
- NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_assertion description "[Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_provenance.
- NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_assertion evidence source_evidence_literature NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_provenance.
- NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_assertion SIO_000772 14595656 NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_provenance.
- NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_assertion wasDerivedFrom befree-20150227 NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_provenance.
- NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_assertion wasGeneratedBy ECO_0000203 NP576661.RAv2-cXA2euqwQfrvS4kQmfrcCigxKLjMJa0cBGnDXo9o130_provenance.