Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_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." NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_assertion evidence source_evidence_literature NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_assertion SIO_000772 9837812 NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_assertion wasDerivedFrom befree-20150227 NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_assertion wasGeneratedBy ECO_0000203 NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP586729.RAxzNmbGvr-Sob0N7HYu5xJKIJN0EdX6r0PjwDgmeZaaI130_provenance.