Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_assertion type Assertion NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_head.
- NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_assertion description "[Cycle sequencing of amplified NDUFS8 cDNA of 20 patients with isolated enzymatic complex I deficiency revealed two compound heterozygous transitions in a patient with neuropathologically proven Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_provenance.
- NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_assertion evidence source_evidence_literature NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_provenance.
- NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_assertion SIO_000772 9837812 NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_provenance.
- NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_assertion wasDerivedFrom befree-2016 NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_provenance.
- NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_assertion wasGeneratedBy ECO_0000203 NP1410084.RAxRzWW9t2xnTh4Va5E-XGXysvmbG9h8VrD3Zhjb2TZMY130_provenance.