Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_assertion description "[In total, 451 patients with AS and 402 ethnically matched healthy controls were genotyped with 51 single-nucleotide polymorphisms (SNP) within the IL-1 gene cluster (specifically located within the IL1A, IL1B, IL1RN, and IL1F5-10 genes based on findings of previous association studies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_assertion evidence source_evidence_literature NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_assertion SIO_000772 18484691 NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_assertion wasDerivedFrom gad-20150221 NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_assertion wasGeneratedBy ECO_0000203 NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123187.RAhi4UUng3N2trR-vxSnca0r2h6L9Xj4_Bg1C90j4P8fo130_provenance.