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Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_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." NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
• 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." provenance.
• 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.
• 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." provenance.
• NP499163.RA5VaIpAaB0IpPO7E-aewu2WMeVklHoeQBGur6ajWebds130_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." NP499163.RA5VaIpAaB0IpPO7E-aewu2WMeVklHoeQBGur6ajWebds130_provenance.
• NP629633.RARZu55c9E_UrgcGIaOqcvsBJMpiPmrIa8mHgX38Rijiw130_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." NP629633.RARZu55c9E_UrgcGIaOqcvsBJMpiPmrIa8mHgX38Rijiw130_provenance.
• NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_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." NP497074.RAKeNsH0IEb-h6S2e7wBzxOzTsjY85YOguckJ_drwjhFM130_provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• NP556118.RAdrYUlvxrS2Mj8bnbwvM7Y8U8bpNcRBovz2TdBppefPI130_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." NP556118.RAdrYUlvxrS2Mj8bnbwvM7Y8U8bpNcRBovz2TdBppefPI130_provenance.
• NP556119.RAo93oh73EVtze6MA-Xgry4dGqXuZyj8T1T2bGIs4LAAI130_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." NP556119.RAo93oh73EVtze6MA-Xgry4dGqXuZyj8T1T2bGIs4LAAI130_provenance.
• NP867718.RAPodcNpPAEc3vY6goq-UvN9_5t0d2zWc3ETgk-JJRUb4130_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." NP867718.RAPodcNpPAEc3vY6goq-UvN9_5t0d2zWc3ETgk-JJRUb4130_provenance.
• NP556114.RANCeJ36BzQ_eYtgp0xNa1VggH06PqbzB1oGz1bQvXEiI130_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." NP556114.RANCeJ36BzQ_eYtgp0xNa1VggH06PqbzB1oGz1bQvXEiI130_provenance.