Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP743334.RAnnf8_CmNs0Oo85ia3eP3gOuxbSvym_zkeDHK9aBQpJQ130_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." NP743334.RAnnf8_CmNs0Oo85ia3eP3gOuxbSvym_zkeDHK9aBQpJQ130_provenance.
• NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_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." NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
• NP671106.RAd8VcOJCctseidCAE7SIhzzYN7AZ1fvbXfr2JXAh9iVs130_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." NP671106.RAd8VcOJCctseidCAE7SIhzzYN7AZ1fvbXfr2JXAh9iVs130_provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• 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." provenance.
• NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_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." NP818808.RAM6c93peYmCLze4cbhrgXWPD4Ghu1Gj54xzAcno50dq0130_provenance.
• NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_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." NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
• NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_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." NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_provenance.
• NP550131.RAg4A49RSJBbuzeMhqDkXA1uVlbPzbC8-_vQwLcXidgQU130_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." NP550131.RAg4A49RSJBbuzeMhqDkXA1uVlbPzbC8-_vQwLcXidgQU130_provenance.
• 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.
• NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_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." NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_provenance.
• NP550134.RA4jkFsS83SAMUUV-WQHb_h7nERZIKxNdshNjiuyqAtus130_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." NP550134.RA4jkFsS83SAMUUV-WQHb_h7nERZIKxNdshNjiuyqAtus130_provenance.