Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_assertion> ?p ?o ?g. }
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- NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_assertion type Assertion NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_head.
- NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_assertion description "[In blinded specimens and colon cancer cell lines with defined mutations, ColoSeq correctly identified 28/28 (100%) pathogenic mutations in MLH1, MSH2, MSH6, PMS2, EPCAM, APC, and MUTYH, including single nucleotide variants (SNVs), small insertions and deletions, and large copy number variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_provenance.
- NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_assertion evidence source_evidence_literature NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_provenance.
- NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_assertion SIO_000772 22658618 NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_provenance.
- NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_assertion wasDerivedFrom befree-2016 NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_provenance.
- NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_assertion wasGeneratedBy ECO_0000203 NP986588.RAQsQX-Ucl5v-1e2dBY01C-Y0niqRAmyesD0aWHNFoOs0130_provenance.