Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_assertion description "[Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_assertion evidence source_evidence_curated NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_assertion SIO_000772 10749987 NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_assertion wasDerivedFrom uniprot-2016 NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_assertion wasGeneratedBy ECO_0000218 NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP754.RAlW0LHpLbRInvancJ7VCdaiE5CG2dKdCeJsO_VsN3PZs130_provenance.