Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_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." NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_assertion evidence source_evidence_literature NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_assertion SIO_000772 16707008 NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_assertion wasDerivedFrom befree-20150227 NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_assertion wasGeneratedBy ECO_0000203 NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP670534.RADi2IiJkhphCS5GLQai7akpnSTkY21XINkT7CszXMeSs130_provenance.