Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_assertion type Assertion NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_head.
- NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_assertion wasGeneratedBy ECO_0000203 NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_provenance.
- NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_assertion wasDerivedFrom befree-2016 NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_provenance.
- NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_assertion SIO_000772 23403405 NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_provenance.
- NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_assertion evidence source_evidence_literature NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_provenance.
- NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_assertion description "[These discoveries indicate that ADHR, XLH, and ARHR represent three related heritable hypophosphatemic diseases that arise from mutations in, or dysregulation of, a single common gene product, FGF23 and, in ARHR and XLH, complimentary DMP1 and PHEX directed events that contribute to abnormal bone mineralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1052335.RA1Dnz8Y50jgt8uF1Bu76FTKzgyxvTIUJmNIl98Ud5YzM130_provenance.