Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_assertion type Assertion NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_head.
- NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_assertion description "[Gain-of-function RET mutations are responsible for multiple endocrine neoplasia syndromes (MEN) 2A and 2B and familial medullary thyroid carcinoma (FMTC), whereas loss-of-function mutations are found in Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_provenance.
- NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_assertion evidence source_evidence_literature NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_provenance.
- NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_assertion SIO_000772 15472167 NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_provenance.
- NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_assertion wasDerivedFrom befree-2016 NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_provenance.
- NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_assertion wasGeneratedBy ECO_0000203 NP463542.RAY5c0C5JMNJ6dx2GKg4bcu2huuwrM_1K173w3Bs-VOVc130_provenance.