Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_assertion description "[In Czech population, only DRB1*03-DQB1*0201 haplotype is significantly associated with increased risk for SLE development: the frequency in SLE group was 44.7% in comparison with 15.2% in controls, P (c) < 0.0001; OR 4.54 CI 95% (2.36-9.09).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_assertion evidence source_evidence_literature NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_assertion SIO_000772 20352225 NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_assertion wasDerivedFrom befree-2016 NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_assertion wasGeneratedBy ECO_0000203 NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.
- befree-2016 importedOn "2016-02-19" NP803220.RADK2rnnFGA1zQsUKtkmffB6kSEruYh33UWb2o4YsIErc130_provenance.