Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion description "[A point mutation or a small deletion of mitochondrial DNA, probably affecting the COX-II gene, may be responsible for the COX deficiency in this case of MERRF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion evidence source_evidence_literature NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion SIO_000772 2549843 NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion wasDerivedFrom befree-20140225 NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_assertion wasGeneratedBy ECO_0000203 NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP810069.RAIRFE7mzTbAZdWdPORkrVJhpHRn3eB-NHjRCQwUBXOyc130_provenance.