Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_assertion> ?p ?o ?g. }
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- NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_assertion type Assertion NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_head.
- NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_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." NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_provenance.
- NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_assertion evidence source_evidence_literature NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_provenance.
- NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_assertion SIO_000772 19581284 NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_provenance.
- NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_assertion wasDerivedFrom befree-2016 NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_provenance.
- NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_assertion wasGeneratedBy ECO_0000203 NP749517.RA80FcGokL4Mrck1B4kuu4x1jcnUVIP1saOmflJkQAVvI130_provenance.