Matches in Nanopublications for { ?s ?p "[We found that genomic alterations in the Wnt signaling pathway were common among all three subtypes; however, unique combinations of pathway alterations including Wnt, VEGF and Notch drove distinct molecular and clinical phenotypes in different CRC subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[We found that genomic alterations in the Wnt signaling pathway were common among all three subtypes; however, unique combinations of pathway alterations including Wnt, VEGF and Notch drove distinct molecular and clinical phenotypes in different CRC subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We found that genomic alterations in the Wnt signaling pathway were common among all three subtypes; however, unique combinations of pathway alterations including Wnt, VEGF and Notch drove distinct molecular and clinical phenotypes in different CRC subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_assertion description "[We found that genomic alterations in the Wnt signaling pathway were common among all three subtypes; however, unique combinations of pathway alterations including Wnt, VEGF and Notch drove distinct molecular and clinical phenotypes in different CRC subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_provenance.
- NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_assertion description "[We found that genomic alterations in the Wnt signaling pathway were common among all three subtypes; however, unique combinations of pathway alterations including Wnt, VEGF and Notch drove distinct molecular and clinical phenotypes in different CRC subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.