Matches in Nanopublications for { ?s ?p "[Hypophosphatasia (HPP) is a clinically heterogeneous rare, inherited disorder of bone and mineral metabolism with extensive allelic heterogeneity in the ALPL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion description "[Hypophosphatasia (HPP) is a clinically heterogeneous rare, inherited disorder of bone and mineral metabolism with extensive allelic heterogeneity in the ALPL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hypophosphatasia (HPP) is a clinically heterogeneous rare, inherited disorder of bone and mineral metabolism with extensive allelic heterogeneity in the ALPL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1158121.RAn9WFhtAoPYCob76ZFYelss_JDKh_atbTgGuqjxMF6KI130_assertion description "[Hypophosphatasia (HPP) is a clinically heterogeneous rare, inherited disorder of bone and mineral metabolism with extensive allelic heterogeneity in the ALPL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158121.RAn9WFhtAoPYCob76ZFYelss_JDKh_atbTgGuqjxMF6KI130_provenance.
- NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion description "[Hypophosphatasia (HPP) is a clinically heterogeneous rare, inherited disorder of bone and mineral metabolism with extensive allelic heterogeneity in the ALPL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- NP1158123.RA47L5ZDZhvAqHM0nBPO09Gb6WNjAMnlko4Tg6sZI5UM8130_assertion description "[Hypophosphatasia (HPP) is a clinically heterogeneous rare, inherited disorder of bone and mineral metabolism with extensive allelic heterogeneity in the ALPL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158123.RA47L5ZDZhvAqHM0nBPO09Gb6WNjAMnlko4Tg6sZI5UM8130_provenance.