Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_assertion> ?p ?o ?g. }
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- NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_assertion type Assertion NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_head.
- NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_assertion description "[Germline mutations in RET are responsible for multiple endocrine neoplasia type 2 (MEN2), an autosomal dominantly inherited cancer syndrome that is characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and parathyroid hyperplasia/adenoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_provenance.
- NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_assertion evidence source_evidence_literature NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_provenance.
- NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_assertion SIO_000772 16707008 NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_provenance.
- NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_assertion wasDerivedFrom befree-20150227 NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_provenance.
- NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_assertion wasGeneratedBy ECO_0000203 NP670806.RAL0j3Qx7VlxUIlItWqx2vNvceY6iJZJFLr6waq7-CjWQ130_provenance.