Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_assertion> ?p ?o ?g. }
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- NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_assertion type Assertion NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_head.
- NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_assertion wasGeneratedBy ECO_0000203 NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_provenance.
- NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_assertion wasDerivedFrom befree-20150227 NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_provenance.
- NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_assertion SIO_000772 10902805 NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_provenance.
- NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_assertion evidence source_evidence_literature NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_provenance.
- NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_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." NP648787.RAq4-Ma6Vcm0dWE8IvUE_3WwVuvD8UOalq5kJq4GsWkmo130_provenance.