Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- befree-2016 importedOn "2016-02-19" NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_assertion wasGeneratedBy ECO_0000203 NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_assertion wasDerivedFrom befree-2016 NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_assertion SIO_000772 21947821 NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_assertion evidence source_evidence_literature NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.
- NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_assertion description "[In all, 171 patients with breast cancer who had HER2 FISH that had increased mean CEP17 copy numbers (> 2.6) were selected for additional chromosome 17 studies that used probes for Smith-Magenis syndrome (SMS), retinoic acid receptor alpha (RARA), and tumor protein p53 (TP53) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926433.RAu7A3VD66TGruyD8k3X2KuaLX5jtPohM9I8fDglVi4AE130_provenance.