Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_assertion> ?p ?o ?g. }
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- NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_assertion type Assertion NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_head.
- NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_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." NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_provenance.
- NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_assertion evidence source_evidence_literature NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_provenance.
- NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_assertion SIO_000772 25345868 NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_provenance.
- NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_assertion wasDerivedFrom befree-2016 NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_provenance.
- NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_assertion wasGeneratedBy ECO_0000203 NP1232688.RADh1-iD72eFbnbmHLi0gW1B2WJF0OKB_v3UtyvQuDizA130_provenance.