Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_assertion> ?p ?o ?g. }
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- NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_assertion type Assertion NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_head.
- NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_assertion description "[Diagnoses included Drash syndrome with Wilms tumor in infancy (3 patients), partial androgen insensitivity resulting from androgen receptor mutations (2), true hermaphroditism (2), chromosomal aberration (1), deficiency of antim�llerian hormone (1), gonadal dysgenesis (1), partial 5 alpha-reductase deficiency caused by a novel point mutation (1), and XX-male syndrome (1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_provenance.
- NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_assertion evidence source_evidence_literature NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_provenance.
- NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_assertion SIO_000772 9329414 NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_provenance.
- NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_assertion wasDerivedFrom befree-20140225 NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_provenance.
- NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_assertion wasGeneratedBy ECO_0000203 NP790991.RACv61fckd61zG4lUW3jSMen28wOyZdC2lzdmck5dWtKY130_provenance.