Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_assertion> ?p ?o ?g. }
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- NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_assertion type Assertion NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_head.
- NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_assertion wasGeneratedBy ECO_0000203 NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_provenance.
- NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_assertion wasDerivedFrom befree-20140225 NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_provenance.
- NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_assertion SIO_000772 23403405 NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_provenance.
- NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_assertion evidence source_evidence_literature NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_provenance.
- NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_assertion description "[However, investigations focusing on the pathogenesis of X-linked hypophosphatemia (XLH), autosomal dominant hypophosphatemic rickets (ADHR), and autosomal recessive hypophosphatemic rickets (ARHR), heritable disorders characterized by abnormal renal phosphate wasting and bone mineralization, have clearly implicated FGF23 as a central factor in osteocytes underlying renal phosphate wasting, documented new molecular pathways regulating FGF23 production, and revealed complementary abnormalities in osteocytes that regulate bone mineralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564487.RAdOLtcnZyt2H9gMFZrBgeOe9y6FdG8F2TvxbsAgffuas130_provenance.