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- NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_assertion type Assertion NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_head.
- NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_assertion description "[X-linked hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency in an inherited disorder of purine metabolism is usually associated with the clinical manifestations of hyperuricemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_provenance.
- NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_assertion evidence source_evidence_literature NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_provenance.
- NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_assertion SIO_000772 25476133 NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_provenance.
- NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_assertion wasDerivedFrom befree-2016 NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_provenance.
- NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_assertion wasGeneratedBy ECO_0000203 NP1244926.RAkAW8ObkBk-wrZ4p4uNjW7ahwBJPn2Y-2Al3-9WMm_uY130_provenance.