Matches in Nanopublications for { ?s ?p "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- NP188176.RA7wmqszEpelbbW85OK2lu0TQ3M8pv76iKYAg7ZDwHPaQ130_assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188176.RA7wmqszEpelbbW85OK2lu0TQ3M8pv76iKYAg7ZDwHPaQ130_provenance.
- assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- NP1069402.RAv90ChmuIjCr2js3QYoNl7l6Giocff6IrDOud8rhONMI130_assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069402.RAv90ChmuIjCr2js3QYoNl7l6Giocff6IrDOud8rhONMI130_provenance.
- NP1069403.RAGizpRph2wvA0lExECDJMQnSsYgAGi4J3MIjz0rHLwNA130_assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069403.RAGizpRph2wvA0lExECDJMQnSsYgAGi4J3MIjz0rHLwNA130_provenance.