Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_assertion description "[As Crohn's disease patients are at increased risk of developing sporadic colorectal cancer, it is conceivable that genetic variability within CARD15 may also play a role in determining susceptibility to this gastrointestinal malignancy in individuals without Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_assertion evidence source_evidence_literature NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_assertion SIO_000772 16510569 NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_assertion wasDerivedFrom befree-2016 NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_assertion wasGeneratedBy ECO_0000203 NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.
- befree-2016 importedOn "2016-02-19" NP538281.RA3NarVTSdIK1nIEnW5CGlJ7y2DLLbxUXi9t5GkVTAj_s130_provenance.