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- source_evidence_literature type ECO_0000212 NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_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." NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_assertion evidence source_evidence_literature NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_assertion SIO_000772 19414146 NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_assertion wasDerivedFrom befree-2016 NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_assertion wasGeneratedBy ECO_0000203 NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.
- befree-2016 importedOn "2016-02-19" NP736393.RAIqSXh-YbVu0wVH5nuugfL5vPYf9fR7WlQhgBxzA1I34130_provenance.