Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_assertion> ?p ?o ?g. }
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- NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_assertion type Assertion NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_head.
- 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.
- NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_assertion evidence source_evidence_literature NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_provenance.
- NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_assertion SIO_000772 16707008 NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_provenance.
- NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_assertion wasDerivedFrom befree-2016 NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_provenance.
- NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_assertion wasGeneratedBy ECO_0000203 NP550133.RAQRvxZ9oMXZ1sUOX5GqlGxiOqmN5AXXhluhnSRcgdG94130_provenance.