Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_assertion> ?p ?o ?g. }
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- NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_assertion type Assertion NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_head.
- NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_assertion wasGeneratedBy ECO_0000203 NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_provenance.
- NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_assertion wasDerivedFrom befree-2016 NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_provenance.
- NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_assertion SIO_000772 10902805 NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_provenance.
- NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_assertion evidence source_evidence_literature NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_provenance.
- NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_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." NP289477.RAwqj4SB7raOhZUMED6d6zEbMc1XCS5i18Gk84MMpQYAI130_provenance.