Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_assertion> ?p ?o ?g. }
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- NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_assertion type Assertion NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_head.
- 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.
- NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_assertion evidence source_evidence_curated NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.
- NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_assertion SIO_000772 11414762 NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.
- NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_assertion wasDerivedFrom ctd_human-20130708 NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.
- NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_assertion wasGeneratedBy ECO_0000218 NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.