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- source_evidence_literature type ECO_0000212 NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_assertion description "[The causative gene (mutated HTT) is widely expressed outside the CNS and several peripheral signs of disease, including weight loss and increased proinflammatory signalling, are often seen; however, their importance in the pathophysiology of Huntington's disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_assertion evidence source_evidence_literature NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_assertion SIO_000772 26466780 NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_assertion wasDerivedFrom befree-2016 NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_assertion wasGeneratedBy ECO_0000203 NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294941.RAQKMsGEhgjZwu-Mbf6liJlwe84PaJbn0eVhiS1gmFWY8130_provenance.