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- source_evidence_literature type ECO_0000212 NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP789950.RAL8X_68kz_377P6xo0mcnim3HeFvb2JMWONJHbIZwMcU130_provenance.
- 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.