Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_assertion description "[Phaeochromocytoma-paraganglioma syndrome can be diagnosed reliably by an immunohistochemical procedure. SDHB, SDHC, and SDHD germline mutation testing is indicated only in patients with SDHB-negative tumours. SDHB immunohistochemistry on phaeochromocytoma]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_assertion evidence source_evidence_literature NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_assertion SIO_000772 19576851 NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_assertion wasDerivedFrom gad-20150221 NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_assertion wasGeneratedBy ECO_0000203 NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151712.RAz_PTxQUDViom1W2P4NXs0ZNsQhGLJJ8meLb_WjKFK8o130_provenance.