Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP345390.RAslzD2JAI7ViRItDEW9XNeph4ehaRnCFu7W0A0WIjzcg130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345390.RAslzD2JAI7ViRItDEW9XNeph4ehaRnCFu7W0A0WIjzcg130_provenance.
• NP543197.RAC3tvqplNhpv6KilD50eP6jwpqJ7f-yyGnRQHvdH3E_A130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP543197.RAC3tvqplNhpv6KilD50eP6jwpqJ7f-yyGnRQHvdH3E_A130_provenance.
• NP817359.RAD-Owv6h5dEVuLSc55d7-jfmFXQoU4JrXBTt9H3OTZpk130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817359.RAD-Owv6h5dEVuLSc55d7-jfmFXQoU4JrXBTt9H3OTZpk130_provenance.
• NP243937.RAjMBvLhmhR02z_Thbs7zYuLGk6VS2Wi_0MJmjBuge8zk130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243937.RAjMBvLhmhR02z_Thbs7zYuLGk6VS2Wi_0MJmjBuge8zk130_provenance.
• NP593308.RATjvqQGzBWHavIF8QX1unJq1sKTlAHSTtVSpoqY7271Y130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593308.RATjvqQGzBWHavIF8QX1unJq1sKTlAHSTtVSpoqY7271Y130_provenance.
• NP717585.RApmfpkDBMqTXUrStNacqtdhspd0Vr-IvxwZzIo3ictF8130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717585.RApmfpkDBMqTXUrStNacqtdhspd0Vr-IvxwZzIo3ictF8130_provenance.
• NP857559.RAvxyizlJV2a5kuGc4ZuJvJWmj4wM3jwFOhBx05JW7s6I130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857559.RAvxyizlJV2a5kuGc4ZuJvJWmj4wM3jwFOhBx05JW7s6I130_provenance.
• NP786350.RAxhBNZdX78E2cjhYiVNvyN__x7O2a-KcDQwoz8N4xPAM130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786350.RAxhBNZdX78E2cjhYiVNvyN__x7O2a-KcDQwoz8N4xPAM130_provenance.
• NP743227.RAvjt-Dk0593YytLLtikU1c4fIUBYZWIl-fZW6oE5IbDc130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743227.RAvjt-Dk0593YytLLtikU1c4fIUBYZWIl-fZW6oE5IbDc130_provenance.
• NP673071.RAJgLlMksUI7txDTqhQn87K2g8jPwfysv45LdZ962SXxU130_assertion description "[An ataxic form of GSS is genetically linked to a mutation at codon 102 (CCG-->CTG) leading to the substitution of leucine for proline, while a `telencephalic` variant of GSS, in which dementia is the predominant symptom and ataxia is minimal, has been described in two kindreds with a mutation at codon 117 (GCA-->GTG) resulting in the substitution of valine for alanine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673071.RAJgLlMksUI7txDTqhQn87K2g8jPwfysv45LdZ962SXxU130_provenance.