Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_assertion> ?p ?o ?g. }
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- NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_assertion type Assertion NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_head.
- 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.
- NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_assertion evidence source_evidence_literature NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_provenance.
- NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_assertion SIO_000772 24260186 NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_provenance.
- NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_assertion wasDerivedFrom befree-2016 NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_provenance.
- NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_assertion wasGeneratedBy ECO_0000203 NP1130138.RABdmnktih0Ssxdf7jXFDqYALWDIahCgmODLMLWxI1sNI130_provenance.