Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_assertion type Assertion NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_head.
- NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_assertion wasGeneratedBy ECO_0000203 NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_assertion wasDerivedFrom befree-20150227 NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_assertion SIO_000772 17466001 NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_assertion evidence source_evidence_literature NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_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." NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.