Matches in Nanopublications for { ?s ?p "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP355137.RAbGe9258GBlmbZvKVSve74R1iUnJF_I8TV7T_2TxtCDY130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355137.RAbGe9258GBlmbZvKVSve74R1iUnJF_I8TV7T_2TxtCDY130_provenance.
- NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236870.RAgGpLslPpLCxcRr3hdV6Gl-Ws1HQEWEB_v7aq-P1kHqc130_provenance.
- NP236856.RABJkOHlrF9yMOH1rZng-6SBUT-zb9ODftYkj_HtJke4U130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236856.RABJkOHlrF9yMOH1rZng-6SBUT-zb9ODftYkj_HtJke4U130_provenance.
- NP236903.RAP0nvo1zQFvd6vSIuG9GSh6ISnBPY7A0UvpCMvY8bUdw130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236903.RAP0nvo1zQFvd6vSIuG9GSh6ISnBPY7A0UvpCMvY8bUdw130_provenance.
- NP1018371.RAPyvEA4s6pOhFHvPkyIQRiaPKa6BXyrkHXXI09GH8Hxw130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018371.RAPyvEA4s6pOhFHvPkyIQRiaPKa6BXyrkHXXI09GH8Hxw130_provenance.
- NP1018370.RA7eto8a6A68gYO9U2nKlOA36xPR9M966yBMbYuFyoB44130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018370.RA7eto8a6A68gYO9U2nKlOA36xPR9M966yBMbYuFyoB44130_provenance.
- NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_assertion description "[Mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene cause hypophosphatasia (HPP), an inborn error of metabolism characterized by defects in bone and teeth mineralization accompanying subnormal levels of serum alkaline phosphatase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018372.RA38HDcsLog9E0Bk1z8LeXfG1QHlP2CMWQXjzYZvqZiCs130_provenance.