Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_assertion description "[Half of hereditary nonpolyposis colon cancer kindreds harbor mutations that inactivate MutLalpha (MLH1*PMS2 heterodimer).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_assertion evidence source_evidence_literature NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_assertion SIO_000772 16873062 NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_assertion wasDerivedFrom befree-2016 NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_assertion wasGeneratedBy ECO_0000203 NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.
- befree-2016 importedOn "2016-02-19" NP561692.RAghq4Sh4ZZC2run9VUUhVXrxyW9Q5xy0HXiiRvGPQ0j0130_provenance.