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- source_evidence_literature type ECO_0000212 NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_assertion description "[Mutations in COQ2 in familial and sporadic multiple-system atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_assertion evidence source_evidence_literature NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_assertion SIO_000772 23758206 NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_assertion wasDerivedFrom befree-20150227 NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_assertion wasGeneratedBy ECO_0000203 NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP887238.RAFzdW2Rbhbi7ySSU5PC1sxpLRhUKPqP9jplLhe3W4hDQ130_provenance.