Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_assertion> ?p ?o ?g. }
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- NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_assertion type Assertion NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_head.
- NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_assertion wasGeneratedBy ECO_0000203 NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_provenance.
- NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_assertion wasDerivedFrom befree-20150227 NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_provenance.
- NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_assertion SIO_000772 23403405 NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_provenance.
- NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_assertion evidence source_evidence_literature NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_provenance.
- NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_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." NP834064.RAjEv1kTeFZQTA6W9HpWU8QZ6_zrddpPW48GYIQO12gAg130_provenance.