Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- befree-2016 importedOn "2016-02-19" NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_assertion wasGeneratedBy ECO_0000203 NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_assertion wasDerivedFrom befree-2016 NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_assertion SIO_000772 10902805 NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_assertion evidence source_evidence_literature NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.
- NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_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." NP289474.RAuPbYR4mx4MeOJwitP-bWOTY3nI5C3B27M_9_TQaWif8130_provenance.