Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_assertion wasGeneratedBy ECO_0000203 NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_assertion wasDerivedFrom befree-2016 NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_assertion SIO_000772 19068082 NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_assertion evidence source_evidence_literature NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.
- NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_assertion description "[Heterozygous germline mutations of the tumor-suppressor gene MEN1 are responsible for multiple endocrine neoplasia type 1 (MEN1), a dominantly inherited familial cancer syndrome characterized by pituitary, parathyroid, and enteropancreatic tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708156.RAg5kcS-vMSv9m2cw6gdZmQOao_is_A5CI-uzQkWrXlzQ130_provenance.