Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_assertion description "[A genetic screen was carried out of the open reading frame of SPRN by direct sequencing in 522 patients with prion disease, including 107 with variant Creutzfeldt-Jakob disease (vCJD), and 861 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_assertion evidence source_evidence_literature NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_assertion SIO_000772 18805828 NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_assertion wasDerivedFrom befree-20150227 NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_assertion wasGeneratedBy ECO_0000203 NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_provenance.