Matches in Nanopublications for { ?s ?p "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_assertion description "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.
- NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_assertion description "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_provenance.
- assertion description "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_assertion description "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_assertion description "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.