Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_assertion description "[We used [18F]2-fluoro-2-deoxy-D-glucose ([18F]FDG) and positron emission tomography (PET) to study regional cerebral glucose utilization (rCMRglc) in four patients with fatal familial insomnia (FFI), a prion disease with a mutation at codon 178 of the prion protein gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_assertion evidence source_evidence_literature NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_assertion SIO_000772 8255458 NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_assertion wasDerivedFrom befree-2016 NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_assertion wasGeneratedBy ECO_0000203 NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1336879.RArgM5_g_elltUGPMNHBxsRTyQn9hdz4qbTZlHFlcCTlQ130_provenance.