Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_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." NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_assertion evidence source_evidence_literature NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_assertion SIO_000772 16707008 NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_assertion wasDerivedFrom befree-20140225 NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_assertion wasGeneratedBy ECO_0000203 NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP183494.RAhyjZFN9S3GkP4gEkF4ai3DD34i5VWcK55SoZnqAam2M130_provenance.