Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_assertion description "[In Lynch syndrome (LS), a dominantly inherited colorectal cancer disease, more than 50 founder pathogenic mutations have been described so far in the mismatch repair (MMR) genes (MLH1, MSH2, MSH6 and PMS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_assertion evidence source_evidence_literature NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_assertion SIO_000772 25345868 NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_assertion wasDerivedFrom befree-2016 NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_assertion wasGeneratedBy ECO_0000203 NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232693.RABWvNEEYoWw1335DFyrzI3wPRAGQ6km2jFXfz72eDdUU130_provenance.