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- NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_assertion type Assertion NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_head.
- NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_assertion wasGeneratedBy ECO_0000203 NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_provenance.
- NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_assertion wasDerivedFrom befree-2016 NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_provenance.
- NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_assertion SIO_000772 17466001 NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_provenance.
- NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_assertion evidence source_evidence_literature NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_provenance.
- NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_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." NP607094.RA7B-N-0VdM8mme7C9T3if51EWgMvU3cRUuvFvLtC7qBU130_provenance.