Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_assertion description "[Others have been recently identified as potential markers of CRC (IFITM1), and the role of others is largely unknown in this disease (CCT3, CCT5, CCT7, and GNA12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_assertion evidence source_evidence_literature NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_assertion SIO_000772 19098285 NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_assertion wasDerivedFrom befree-20140225 NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_assertion wasGeneratedBy ECO_0000203 NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP465900.RAlioxTi6qCZaMHglWlC_Tw-EhMviGXB5gKPNg6siOy_4130_provenance.