Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_assertion description "[ACVR2 is mutated at its exon 10 polyadenine tract in >80% of MSI-H colon cancers, coinciding with loss of protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_assertion evidence source_evidence_literature NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_assertion SIO_000772 17258738 NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_assertion wasDerivedFrom befree-20140225 NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_assertion wasGeneratedBy ECO_0000203 NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP778494.RAlRWr38z-s6PnxGdG8PbbKwtwuFC2dSGLcEVXYMSQaIA130_provenance.