Matches in Nanopublications for { ?s ?p "[They also confirm that the extremely high phenotypic heterogeneity observed in patients with hypophosphatasia was due mainly to variable residual enzymatic activities allowed by missense mutations found in the human TNSALP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1101.RAsjF6fh8szYLB0XxJg8WjsdTYenUGEUihsIL0EBapBHg130_assertion description "[They also confirm that the extremely high phenotypic heterogeneity observed in patients with hypophosphatasia was due mainly to variable residual enzymatic activities allowed by missense mutations found in the human TNSALP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1101.RAsjF6fh8szYLB0XxJg8WjsdTYenUGEUihsIL0EBapBHg130_provenance.
- NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_assertion description "[They also confirm that the extremely high phenotypic heterogeneity observed in patients with hypophosphatasia was due mainly to variable residual enzymatic activities allowed by missense mutations found in the human TNSALP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190.RACD-Dywj1K0chsnqdoJ1XJJgiDTyoGIpELh6Fc5CwBQc130_provenance.
- NP252931.RArh5UUGgeAVh7v4ILDIP_8LRgcqsVQDX9E2mUIbHcnpQ130_assertion description "[They also confirm that the extremely high phenotypic heterogeneity observed in patients with hypophosphatasia was due mainly to variable residual enzymatic activities allowed by missense mutations found in the human TNSALP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252931.RArh5UUGgeAVh7v4ILDIP_8LRgcqsVQDX9E2mUIbHcnpQ130_provenance.