Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_assertion type Assertion NP1003259.RA0vkX0M48O6J4CLyMuFqK0B3ScgpRyOyaRBghaM-xLno130_head.
- 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.