Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_assertion> ?p ?o ?g. }
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- NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_assertion type Assertion NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_head.
- NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_assertion description "[Mutations in Dax-1 cause adrenal hypoplasia congenita, a disorder that is characterized by adrenal insufficiency and hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_provenance.
- NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_assertion evidence source_evidence_literature NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_provenance.
- NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_assertion SIO_000772 9658405 NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_provenance.
- NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_assertion wasDerivedFrom befree-2016 NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_provenance.
- NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_assertion wasGeneratedBy ECO_0000203 NP1399008.RANJ6BP6qq4H3q3wspD-5v7PGoAZgfi4rUIPo56aPAt14130_provenance.