Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_assertion description "[Combined analyses of both cohorts has demonstrated that the incidence of SNP at 5'UTR-25 was 41% (95 of 229), and its A/A genotype (9%, 20 of 229) was observed exclusively in non-Hispanic Caucasians, and 19 of these cases were diagnosed with nodal metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_assertion evidence source_evidence_literature NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_assertion SIO_000772 17981610 NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_assertion wasDerivedFrom befree-20150227 NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_assertion wasGeneratedBy ECO_0000203 NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP432088.RAtQ4ibimrgKrh2kKvLfsCAHNQvLVZ4YHEOoKV72WsiC4130_provenance.