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- NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_assertion type Assertion NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_head.
- NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_assertion wasGeneratedBy ECO_0000203 NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_provenance.
- NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_assertion wasDerivedFrom befree-2016 NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_provenance.
- NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_assertion SIO_000772 24402736 NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_provenance.
- NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_assertion evidence source_evidence_literature NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_provenance.
- NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_assertion description "[In 2002, germline HRPT2 (also known as CDC73) mutation was reported as the cause of hyperparathyroidism-jaw tumor (HPT-JT) syndrome, an autosomal dominant hereditary tumor syndrome associated with a lifetime risk of parathyroid carcinoma approaching 15 %.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1143163.RAjIHFY1RbHck_QCx4foEfUmWsTzzO0e8vPDYCFVE7A_w130_provenance.