Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_assertion wasGeneratedBy ECO_0000203 NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_assertion wasDerivedFrom befree-20150227 NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_assertion SIO_000772 14532116 NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_assertion evidence source_evidence_literature NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.
- NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_assertion description "[Similar results were observed in humans affected with sporadic and variant Creutzfeldt-Jakob disease, implicating for the first time the caspase-12 dependent pathway in a neurodegenerative disease in vivo, and thus offering novel potential targets for the treatment of prion disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014636.RAhbktD_0LI9T9S_oJpu4XU9ucSCo5U9HYPsIzC4K3A3U130_provenance.