Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_assertion description "[Patients in whom no mutation is identified through this mutation protocol, may be sub-cohorts representing a different FAP pathogenesis including MYH associated polyposis and somatic cell mosaicism for APC gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_assertion evidence source_evidence_literature NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_assertion SIO_000772 19414146 NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_assertion wasDerivedFrom befree-20140225 NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_assertion wasGeneratedBy ECO_0000203 NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP879799.RAUXt5wUyVnK-zPqnpwFrndW7tkyh9xSUIceN0iy4gQgE130_provenance.