Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_assertion> ?p ?o ?g. }
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- NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_assertion type Assertion NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_head.
- NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_assertion description "[MEN 2B (multiple endocrine neoplasia type 2B) is an autosomal dominant cancer syndrome caused by an oncogenic form of the receptor tyrosine kinase REarranged during transfection (RET).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.
- NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_assertion evidence source_evidence_literature NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.
- NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_assertion SIO_000772 17599050 NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.
- NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_assertion wasDerivedFrom befree-20140225 NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.
- NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_assertion wasGeneratedBy ECO_0000203 NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.