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- source_evidence_literature type ECO_0000212 NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_assertion description "[A SNP-based risk scoring system, identified here by GWAS analyses, may provide a useful adjunct to clinical parameters for predicting the natural history of UC. Furthermore, discovery of genetic processes underlying disease severity may help to identify p]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_assertion evidence source_evidence_literature NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_assertion SIO_000772 20848476 NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_assertion wasDerivedFrom gad-20150221 NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_assertion wasGeneratedBy ECO_0000203 NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP186027.RA7gn55QqSr0iAhUtoQljEV4K62LiZz38jlknEMQ4-zpE130_provenance.