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- NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_assertion type Assertion NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_head.
- NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_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." NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_provenance.
- NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_assertion evidence source_evidence_literature NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_provenance.
- NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_assertion SIO_000772 15472167 NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_provenance.
- NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_assertion wasDerivedFrom befree-2016 NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_provenance.
- NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_assertion wasGeneratedBy ECO_0000203 NP463539.RAczp-Wrbdhuol5FerSIG_jbnKkJRbFtRZZ4MHJO3xJgc130_provenance.