Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_assertion description "[The majority of Smad4 gene mutations in human cancer are missense, nonsense, and frameshift mutations at the mad homology 2 region (MH2), which interfere with the homo-oligomer formation of Smad4 protein and the hetero-oligomer formation between Smad4 and Smad2 proteins, resulting in disruption of TGFbeta signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_assertion evidence source_evidence_literature NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_assertion SIO_000772 12821112 NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_assertion wasDerivedFrom befree-20150227 NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_assertion wasGeneratedBy ECO_0000203 NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP543416.RA2tq_Ipoxyu1-ebzOyw8cnaOZxC0u0jEpxwk0kuRO79s130_provenance.