Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_assertion> ?p ?o ?g. }
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- NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_assertion type Assertion NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_head.
- NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_assertion description "[Thus these APP and PRIP mutations are rare in both FAD and nonfamilial AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_provenance.
- NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_assertion evidence source_evidence_literature NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_provenance.
- NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_assertion SIO_000772 1679288 NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_provenance.
- NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_assertion wasDerivedFrom befree-20140225 NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_provenance.
- NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_assertion wasGeneratedBy ECO_0000203 NP321307.RA9gaZWBY2VSSJx2suF49pZ9fown194-2BTmXrFYRTZBk130_provenance.