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- NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_assertion type Assertion NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_head.
- 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.
- NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_assertion evidence source_evidence_literature NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_provenance.
- NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_assertion SIO_000772 16707008 NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_provenance.
- NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_assertion wasDerivedFrom befree-2016 NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_provenance.
- NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_assertion wasGeneratedBy ECO_0000203 NP550130.RA9YlHgS8qT8vkmW4rWg5fA0lmh2zmkG8jkTBvXv7vlx4130_provenance.