Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_assertion> ?p ?o ?g. }
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- NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_assertion type Assertion NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_head.
- NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_assertion description "[X-linked hypophosphatemic rickets/osteomalacia (XLH), autosomal dominant and recessive hypophosphatemic rickets/osteomalacia (ADHR and ARHR) share common clinical features including high fibroblast growth factor 23 (FGF23) levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_provenance.
- NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_assertion evidence source_evidence_literature NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_provenance.
- NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_assertion SIO_000772 19581284 NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_provenance.
- NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_assertion wasDerivedFrom befree-20150227 NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_provenance.
- NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_assertion wasGeneratedBy ECO_0000203 NP789440.RAPQj97nnCAvNvlaMegSk2gLDr6D9_jzJk08TgKPN1Yuc130_provenance.