Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_assertion> ?p ?o ?g. }
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- NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_assertion type Assertion NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_head.
- NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_assertion wasGeneratedBy ECO_0000203 NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_provenance.
- NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_assertion wasDerivedFrom befree-2016 NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_provenance.
- NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_assertion SIO_000772 10902805 NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_provenance.
- NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_assertion evidence source_evidence_literature NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_provenance.
- NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_assertion description "[Mutations of the pituitary transcription factor Prop-1, which is responsible for the syndrome of Ames dwarfism in mice, are being increasingly recognized as a cause of combined pituitary hormone deficiency in humans, although ACTH deficiency has been described only once.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289479.RAe-xur7hTV9Pg7RbhVgwWdRml4ZfVpiBWN432erQOypI130_provenance.