Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion description "[To investigate whether the PRND polymorphisms are associated with an increased risk for developing sporadic CJD in the Korean population, we compared the genotype and allele frequencies of PRND polymorphisms in 110 sporadic CJD patients with those in 102 healthy Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion evidence source_evidence_literature NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion SIO_000772 15933804 NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion wasDerivedFrom befree-20140225 NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion wasGeneratedBy ECO_0000203 NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.