Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_assertion type Assertion NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_head.
- NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_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." NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_provenance.
- NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_assertion evidence source_evidence_literature NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_provenance.
- NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_assertion SIO_000772 9329414 NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_provenance.
- NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_assertion wasDerivedFrom befree-20150227 NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_provenance.
- NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_assertion wasGeneratedBy ECO_0000203 NP250934.RA_O8VrSa1CIRlsTV2UzL1-N0pnbe-pUBNHjeH_D6Prq4130_provenance.