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- source_evidence_literature type ECO_0000212 NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_assertion wasGeneratedBy ECO_0000203 NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_assertion wasDerivedFrom lhgdn-20090331 NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_assertion SIO_000772 15235026 NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_assertion evidence source_evidence_literature NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.
- NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_assertion description "[A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208901.RAFBpyBf4oAL4b2dLyryh-YtARittj6-GaLjpYdoOyIKo130_provenance.