Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP208603.RACR4hDxU3bbegjfu4nqkLT0Ur8Y5zFlwcKNO83MFoN88130_provenance.