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- source_evidence_literature type ECO_0000212 NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_assertion description "[We sought to determine the contribution of C9orf72 repeat expansions, recently discovered as a cause of frontotemporal dementia and amyotrophic lateral sclerosis, in a large number of Parkinson's disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_assertion evidence source_evidence_literature NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_assertion SIO_000772 22721568 NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_assertion wasDerivedFrom befree-2016 NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_assertion wasGeneratedBy ECO_0000203 NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.
- befree-2016 importedOn "2016-02-19" NP991951.RAUiA7zq_L0IWAtrEHMoW8OCvxpKLUbnIgZtXtX1IBRBM130_provenance.