Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP616467.RAQVY_BnNNqCMa6w7N1ekJGMVuOZjIEF4EGH87pGm64Eg130_provenance.