Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_assertion description "[To investigate the presence of mutations in the open reading frame (ORF), as well as on the 5' and 3', flanking regions of the SRY gene in patients with mixed gonadal dysgenesis (MGD) or with Turner syndrome (TS) and Y mosaicism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_assertion evidence source_evidence_literature NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_assertion SIO_000772 15223166 NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_assertion wasDerivedFrom befree-2016 NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_assertion wasGeneratedBy ECO_0000203 NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.
- befree-2016 importedOn "2016-02-19" NP450152.RA57klpxGLl4Rb6KuQdhmUnjIY8zVuVGM7r0iGlTB_804130_provenance.