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- NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_assertion type Assertion NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_head.
- NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_assertion wasGeneratedBy ECO_0000203 NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_provenance.
- NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_assertion wasDerivedFrom befree-20140225 NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_provenance.
- NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_assertion SIO_000772 17466001 NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_provenance.
- NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_assertion evidence source_evidence_literature NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_provenance.
- NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_assertion description "[Patients lacked mutations in other genes known to cause ACTH resistance, including AAAS for patients diagnosed with triple A syndrome and MC2R and MRAP for patients diagnosed with familial glucocorticoid deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796286.RARBCBH-q1FDtI5NxjdDRhspn-iScik31YiCVgAWQyjvY130_provenance.