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- source_evidence_literature type ECO_0000212 NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_assertion description "[Routine germline MEN1 mutation testing of all cases of " classical " MEN1, familial hyperparathyroidism, and sporadic hyperparathyroidism with one other MEN1 related condition is justified by national testing services.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_assertion evidence source_evidence_literature NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_assertion SIO_000772 15635078 NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_assertion wasDerivedFrom lhgdn-20090331 NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_assertion wasGeneratedBy ECO_0000203 NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP137158.RAWztVi6C-ga4DoMg18bMDma9lQ7usTyI9aHlig3iOx0o130_provenance.