Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_assertion description "[An unacceptable recurrence/persistence rate (80%) associated with increasingly difficult re-operations and risk of parathyroid carcinoma in the setting of germline mutations of HRPT2 gene with familial hyperparathyroidism suggest that a more aggressive operative approach should be undertaken in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_assertion evidence source_evidence_literature NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_assertion SIO_000772 18436011 NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_assertion wasDerivedFrom befree-20150227 NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_assertion wasGeneratedBy ECO_0000203 NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP943640.RAi3O8IOrkYbwuU_UNp21X2PBNRMWMS_1sDDJESLJpRNQ130_provenance.