Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_assertion description "[Univariate testing of these genes using non-adjacent, non-neoplastic sections from UC-CRC cases indicated that associations between p16, RUNX3, MINT1, MINT31, E-cadherin, and COX-2 and UC-CRC remained significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_assertion evidence source_evidence_literature NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_assertion SIO_000772 20160714 NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_assertion wasDerivedFrom befree-2016 NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_assertion wasGeneratedBy ECO_0000203 NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.
- befree-2016 importedOn "2016-02-19" NP794214.RAxOF3BlSlsfC0dQwQ4JORlf6eeQgeso-0VoYr-qaVAS4130_provenance.