Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_assertion description "[Fifty-six single-nucleotide polymorphisms (SNPs) across STAT1 and STAT4 on chromosome 2 were genotyped using the Illumina platform, as part of an extensive association study in a large collection of 9,923 lupus patients and control subjects from different racial groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_assertion evidence source_evidence_literature NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_assertion SIO_000772 19333953 NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_assertion wasDerivedFrom gad-20150221 NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_assertion wasGeneratedBy ECO_0000203 NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123763.RAoAK1NGQK-6bBiDNBq5JnfwsGyw5eAXkmXUZGIHLiclY130_provenance.