Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_assertion description "[When the nine promoter/5' untranslated region [UTR] and five htSNP genotypes were combined into a 14-SNP haplotype, a single haplotype, -460C, -417T, -172C, -165C, -160C, -152A, -141A, -116A, +405C, +674T, +4618C, +5092A, +9162C, +9512C was found to be significantly associated with the PDR group (OR = 18.45 [2.35, 144.67], P = 0.00622).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_assertion evidence source_evidence_literature NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_assertion SIO_000772 18441306 NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_assertion wasDerivedFrom befree-20150227 NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_assertion wasGeneratedBy ECO_0000203 NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP432260.RAHaqCIoevGCEY-_H92JTid6GLWjugyRhCcptRjyaiNHU130_provenance.