Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_assertion description "[To evaluate whether sequence variants of NTHL1, NEIL1, NEIL2, MPG, TDG, UNG and SMUG1 genes might act as CRC susceptibility alleles, we screened the coding sequence and intron-exon boundaries of these genes in 94 familial CRC cases in which involvement of known genes had been excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_assertion evidence source_evidence_literature NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_assertion SIO_000772 17029639 NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_assertion wasDerivedFrom befree-2016 NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_assertion wasGeneratedBy ECO_0000203 NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP573510.RAlb9FygOEQ04R1QLtTHsWGWKGcTRHLgdr2HIsYai-UoQ130_provenance.