Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_assertion> ?p ?o ?g. }
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- NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_assertion type Assertion NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_head.
- 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.
- NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_assertion evidence source_evidence_curated NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_provenance.
- NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_assertion SIO_000772 11414762 NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_provenance.
- NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_assertion wasDerivedFrom ctd_human-20150221 NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_provenance.
- NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_assertion wasGeneratedBy ECO_0000218 NP25713.RAfcnXQHxSD2TQs4oXvtMcPr7bagCCbaEzCbdeDivU3QA130_provenance.