Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_assertion> ?p ?o ?g. }
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- NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_assertion type Assertion NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_head.
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- NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_assertion wasDerivedFrom uniprot-20150221 NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_provenance.
- NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_assertion SIO_000772 15531542 NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_provenance.
- NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_assertion evidence source_evidence_curated NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_provenance.
- NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_assertion description "[A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418.RASikX8CjFMO8vNJLBJWj-z4CsXkV9sJEUc9on-4PZSJM130_provenance.