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- source_evidence_literature type ECO_0000212 NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_assertion description "[The OPA1 gene, encoding a dynamin-like mitochondrial GTPase, is involved in autosomal dominant optic atrophy (ADOA, OMIM #165500).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_assertion evidence source_evidence_literature NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_assertion SIO_000772 19389487 NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_assertion wasDerivedFrom befree-2016 NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_assertion wasGeneratedBy ECO_0000203 NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.
- befree-2016 importedOn "2016-02-19" NP734325.RADk6DHtGgo6C5kM_OCfkO8Eg5y4B68uX4OuR6bhO2py0130_provenance.