Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_assertion wasGeneratedBy ECO_0000203 NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_assertion wasDerivedFrom befree-20150227 NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_assertion SIO_000772 24562971 NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_assertion evidence source_evidence_literature NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.
- NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_assertion description "[To test this hypothesis, we studied 39 potentially functional single-nucleotide polymorphisms (SNPs) in eight genes (CYP2R1, CYP3A4, CYP24A1, CYP27A1, CYP27B1, GC, DHCR7, and VDR) in 961 AA CRC cases and 838 healthy AA controls from Chicago and North Carolina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769652.RATCMBoa4IV5FkqvfrczyhPyIgMhONh4U8jfOz_r933e8130_provenance.