Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_assertion description "[Additionally, our data revealed POU1F1 mutations in three patients who were diagnosed as having ACTH deficiency but who, on further evaluation, were found to have normal cortisol secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_assertion evidence source_evidence_literature NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_assertion SIO_000772 15928241 NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_assertion wasDerivedFrom befree-2016 NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_assertion wasGeneratedBy ECO_0000203 NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.
- befree-2016 importedOn "2016-02-19" NP497222.RAR3qHOHc500hMo3OC0fU7G6hcxQONgz8Q3oNg1anoo9g130_provenance.