Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_assertion description "[Most genomic alterations in patients with SDH-deficient RCCs involve the SDHB subunit, and the associated renal tumors have loss of immunohistochemical SDHB expression and distinctive morphologic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_assertion evidence source_evidence_literature NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_assertion SIO_000772 25724004 NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_assertion wasDerivedFrom befree-2016 NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_assertion wasGeneratedBy ECO_0000203 NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266809.RAf3wqC_C0_ZoJGZWtdF_1X-V4hDpI2mftirCCaPrgfxk130_provenance.