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- source_evidence_literature type ECO_0000212 NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_assertion description "[Since, we observed a higher incidence of a single nucleotide polymorphism (SNP) at the -25 position in the 5'untranslated region (5'UTR-25) of RPH3AL, we performed the genotyping analysis of this SNP in a retrospective CRC cohort (n=134) to assess their clinical importance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_assertion evidence source_evidence_literature NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_assertion SIO_000772 17981610 NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_assertion wasDerivedFrom befree-20150227 NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_assertion wasGeneratedBy ECO_0000203 NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824807.RAUKVynSahX8oxGdHvU9tFZnU7PdTCGda126AQ-2o1FvQ130_provenance.