Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_assertion description "[Here we show that expression of COX10 from a retroviral vector complements the COX deficiency in a patient with anemia and Leigh Syndrome, and in a patient with anemia, sensorineural deafness and fatal infantile hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_assertion evidence source_evidence_literature NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_assertion SIO_000772 12928484 NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_assertion wasDerivedFrom befree-20150227 NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_assertion wasGeneratedBy ECO_0000203 NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP323382.RAmPI9O_3FuG2h11IDx6zNbshhId_ZkILZRQIJNlxd_7g130_provenance.