Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_assertion type Assertion NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_head.
- NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_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." NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_provenance.
- NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_assertion evidence source_evidence_literature NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_provenance.
- NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_assertion SIO_000772 22658618 NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_provenance.
- NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_assertion wasDerivedFrom befree-2016 NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_provenance.
- NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_assertion wasGeneratedBy ECO_0000203 NP986591.RALvB860edYMavCAmoe5O2I-xUFaY4jxZrolKPQlo3C1w130_provenance.