Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_assertion> ?p ?o ?g. }
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- NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_assertion type Assertion NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_head.
- NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_assertion description "[We also tested for the APP codon 693 mutation associated with hereditary cerebral hemorrhage with amyloidosis-Dutch type, for PRIP gene missense mutations at codons 102, 117, and 200, and for the PRIP insertion mutations which are associated with Creutzfeld-Jakob disease and Gerstmann-Straussler Scheinker syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_provenance.
- NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_assertion evidence source_evidence_literature NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_provenance.
- NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_assertion SIO_000772 1679288 NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_provenance.
- NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_assertion wasDerivedFrom befree-20140225 NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_provenance.
- NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_assertion wasGeneratedBy ECO_0000203 NP581395.RAootIVRT4LyFbiJT-q1Ltkl-U8c2Cmuz9BTafelrS8G8130_provenance.