Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP512405.RAYlcigR0bHYT_cyRspTcRC9gbtE9-NgLQNsbLCzZ0iMQ130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512405.RAYlcigR0bHYT_cyRspTcRC9gbtE9-NgLQNsbLCzZ0iMQ130_provenance.
• NP875967.RAUkSWRtzwoGsndbkft8EF9DF_aWRnF2J7EYIqHs5zjd4130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875967.RAUkSWRtzwoGsndbkft8EF9DF_aWRnF2J7EYIqHs5zjd4130_provenance.
• NP6723.RABkws-_YLaGvb8kepnc-6QQibRtt71xCZ0DWAWGLAIzM130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6723.RABkws-_YLaGvb8kepnc-6QQibRtt71xCZ0DWAWGLAIzM130_provenance.
• NP869423.RAbn8jeHap2yJPvi7KCA1lsmCMw2aMAX0ZaRGSmaJnac4130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869423.RAbn8jeHap2yJPvi7KCA1lsmCMw2aMAX0ZaRGSmaJnac4130_provenance.
• NP321754.RAz9qUqRI4CeT0cWOsFd9aJRQtMKb1xxMfmaDVUkGOSNg130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321754.RAz9qUqRI4CeT0cWOsFd9aJRQtMKb1xxMfmaDVUkGOSNg130_provenance.
• assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP843056.RAdY6W9upxJuzV2bro7HMnvhR1FnW0j8CBX3Z-EanKQP8130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843056.RAdY6W9upxJuzV2bro7HMnvhR1FnW0j8CBX3Z-EanKQP8130_provenance.
• assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP761448.RArGM-ud3plWIMs7AVVOsZK0FL1n22FKWp_LHVXeWMV5w130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761448.RArGM-ud3plWIMs7AVVOsZK0FL1n22FKWp_LHVXeWMV5w130_provenance.
• NP802681.RACJj5I7CgRINmBL6dlYOt71OCbg2g1MwtvEOVvEb68FM130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802681.RACJj5I7CgRINmBL6dlYOt71OCbg2g1MwtvEOVvEb68FM130_provenance.
• NP316015.RAojQdWXsZJH50DhtY3k1QaqtwRb751FS0f76DonZzFqo130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316015.RAojQdWXsZJH50DhtY3k1QaqtwRb751FS0f76DonZzFqo130_provenance.
• NP802684.RAfMChILkSByMlQTJRDw5o0ibel9-fku4NX_GYllleiWw130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802684.RAfMChILkSByMlQTJRDw5o0ibel9-fku4NX_GYllleiWw130_provenance.
• NP6160.RAnceCYLrCIuA1635-CHjIguBwX_cNGwyQeLvvypD8RJc130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6160.RAnceCYLrCIuA1635-CHjIguBwX_cNGwyQeLvvypD8RJc130_provenance.
• NP842692.RAPkSICtmbm4Rq95nx4tZ5IboXVj3Bkyl4yyq9BEHFWPE130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842692.RAPkSICtmbm4Rq95nx4tZ5IboXVj3Bkyl4yyq9BEHFWPE130_provenance.
• NP940676.RAOrlgGzKKWHHW4CRGEiCD4RB8C-afQkfC9xzEic9VRJ4130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940676.RAOrlgGzKKWHHW4CRGEiCD4RB8C-afQkfC9xzEic9VRJ4130_provenance.
• NP802682.RAzfu6D3rexgeUd5olUCpbgf0rJW-jiA-ls2zCboRmZMs130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802682.RAzfu6D3rexgeUd5olUCpbgf0rJW-jiA-ls2zCboRmZMs130_provenance.
• NP802683.RA0ZMsPGuebx76LmkxwNPAo6NyzOWdDYU_zBo-Dk4QESA130_assertion description "[There are 35 missense mutations among 68 different mutations in the TPP1 gene, which encodes tripeptidyl peptidase I (TPPI), a lysosomal aminopeptidase associated with classic late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802683.RA0ZMsPGuebx76LmkxwNPAo6NyzOWdDYU_zBo-Dk4QESA130_provenance.