Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP418740.RABwyvEOfheTtcxIUs2Cm5jVZ45TqfIDzDAAh7KeslIxY130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418740.RABwyvEOfheTtcxIUs2Cm5jVZ45TqfIDzDAAh7KeslIxY130_provenance.
• NP713804.RAqNjpA6yNR9mdKUwyNwFYB1HjTk0iX9pQvCmoCT6rxNI130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713804.RAqNjpA6yNR9mdKUwyNwFYB1HjTk0iX9pQvCmoCT6rxNI130_provenance.
• NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164653.RA6heOgXtDl18fG5Ef4fYB77XQhh1JGjpkG2xum2-l0ok130_provenance.
• NP462680.RAXsCxNeB6Itr0BOMhPAGRPwl8U6CvRYyxST2mD5fDVNc130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462680.RAXsCxNeB6Itr0BOMhPAGRPwl8U6CvRYyxST2mD5fDVNc130_provenance.
• NP869380.RA7uebX2kBEv4HQK_quRStNBtbHUhecoBpZ_wh0vj0tPo130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869380.RA7uebX2kBEv4HQK_quRStNBtbHUhecoBpZ_wh0vj0tPo130_provenance.
• NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
• NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647339.RAS2l1o0gu0lg-T5kflDFNsIQrAJtQmaOa6141REwFCdY130_provenance.
• NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567325.RAE3BTQn6pbCdFEXPGUaNBTV3iEitu_tSEY99M2fHtc6o130_provenance.
• assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1414115.RAX4tnDK3tYsJj0spCmuNqtXlshf15wMjqepzu-z1ZhDg130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414115.RAX4tnDK3tYsJj0spCmuNqtXlshf15wMjqepzu-z1ZhDg130_provenance.
• NP1414116.RAVmB0gujz3N6iBKu_KhegIiWKrAjPLXqE8NW6tO21ckI130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414116.RAVmB0gujz3N6iBKu_KhegIiWKrAjPLXqE8NW6tO21ckI130_provenance.
• NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414117.RAXGE1Tr_a148nlKgBvPcE0o4u_8V5OvBLe2pzMYDRoaA130_provenance.
• NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414119.RAYPgaHsJAp2BRLsQA1ytE1ADCEg3Ya1GPI7D5iDHES2c130_provenance.
• NP437091.RAmcTSuANrH1vEpnkG1x8EvOQlNRSe8JbcCsPCAKpslRE130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437091.RAmcTSuANrH1vEpnkG1x8EvOQlNRSe8JbcCsPCAKpslRE130_provenance.
• NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437095.RAm8d-LVkosDWd6hgNm6yCM49PXE99LlVEmkc_KamiQkw130_provenance.
• NP1414114.RAqXqb0Zt9Imoor4t6xofKpbiuMq-8SMLXvtMJz7V0EYk130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414114.RAqXqb0Zt9Imoor4t6xofKpbiuMq-8SMLXvtMJz7V0EYk130_provenance.
• NP437099.RA0qlNYcxmf44Nx72CWuEogEk-4R6lXN10wpCO7Sv_Xuo130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437099.RA0qlNYcxmf44Nx72CWuEogEk-4R6lXN10wpCO7Sv_Xuo130_provenance.
• NP437104.RA3_W7KBQ4fsNVAm55pjofSjTg6taNXBaGXSohkl-rHvI130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437104.RA3_W7KBQ4fsNVAm55pjofSjTg6taNXBaGXSohkl-rHvI130_provenance.
• NP437114.RAwfMFPNpOLYRGh4IN493qv9fHxK64GXfg_ChHDz1zbis130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437114.RAwfMFPNpOLYRGh4IN493qv9fHxK64GXfg_ChHDz1zbis130_provenance.
• NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647428.RA__2H1o03EOLuz_sUaLBsylj8MEBm_rI_zpFfGpPhz8s130_provenance.
• NP1414109.RAGZ3jRFAMd5DV6jhYFMNgN_7e27nXsZYrHE5mQHPNSZQ130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414109.RAGZ3jRFAMd5DV6jhYFMNgN_7e27nXsZYrHE5mQHPNSZQ130_provenance.
• NP1414113.RA6yPBDzn4mueLbTr98MKDLLfMsenHnUubTpMIIgz5HyU130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414113.RA6yPBDzn4mueLbTr98MKDLLfMsenHnUubTpMIIgz5HyU130_provenance.