Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion> ?p ?o ?g. }
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- NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion type Assertion NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_head.
- NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion description "[DAX1 mutations were found in 58% (37 of 64) of 46,XY phenotypic boys referred with adrenal hypoplasia and in all boys (eight of eight) with hypogonadotropic hypogonadism and a family history suggestive of adrenal failure in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_provenance.
- NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion evidence source_evidence_literature NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_provenance.
- NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion SIO_000772 16684822 NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_provenance.
- NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion wasDerivedFrom befree-20150227 NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_provenance.
- NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_assertion wasGeneratedBy ECO_0000203 NP231090.RAXgmaFJIyrKO5m9CF3eFoc4gR_m2iuLeaD62hzZH7rmE130_provenance.