Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_assertion> ?p ?o ?g. }
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- NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_assertion type Assertion NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_head.
- NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_assertion description "[XX female gonadal dysgenesis (XX-GD) is a rare, genetically heterogeneous disorder characterized by lack of spontaneous pubertal development, primary amenorrhea, uterine hypoplasia, and hypergonadotropic hypogonadism as a result of streak gonads.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.
- NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_assertion evidence source_evidence_literature NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.
- NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_assertion SIO_000772 21963259 NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.
- NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_assertion wasDerivedFrom befree-20140225 NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.
- NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_assertion wasGeneratedBy ECO_0000203 NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.