Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_assertion type Assertion NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_head.
- NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_assertion description "[Despite the clinical diversity and atypical laboratory findings seen in familial CJD with the codon 200 mutation, these neuroimaging studies suggest that common regional distributions and a common pathogenesis might underlie the clinical progression both in sporadic CJD and in familial CJD with the codon 200 mutation in the prion protein gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_provenance.
- NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_assertion evidence source_evidence_literature NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_provenance.
- NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_assertion SIO_000772 15850581 NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_provenance.
- NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_assertion wasDerivedFrom befree-2016 NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_provenance.
- NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_assertion wasGeneratedBy ECO_0000203 NP491357.RAH-1kqWPL8H2n9bqMqGxEunJYkM_PHepzDi8-ipyB6lI130_provenance.