Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.
- 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.
- ctd_human-20130708 importedOn "2013-07-24" NP25881.RA-2iRemkkMux0PnivtWpJOwOeGNvTaL0_5vt_VCKRFek130_provenance.