Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_assertion description "[Our study provides the first demonstration of the association of the polymorphism of the MHC2TA gene with genetic risk for AAD that appears to be independent from the well-known association with the polymorphism of HLA class II genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_assertion evidence source_evidence_literature NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_assertion SIO_000772 16849401 NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_assertion wasDerivedFrom gad-20130706 NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_assertion wasGeneratedBy ECO_0000203 NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP64918.RApow6anyPBkNfI4M2tIfV-RIIto0kR3v_PHPJprdInzE130_provenance.