Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_assertion description "[The genomic typing for DRB1, DRB3, DRB4, DRB5, DQA1, DQB1 and DPB1 genes revealed an increased frequency of the DRB1*0701; DQA1*0201; DQB1*0201 haplotype (23.5 vs 9.9% of the controls) and of DPB*0201 allele (42.3 vs 13.2% of controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_assertion evidence source_evidence_literature NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_assertion SIO_000772 7483776 NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_assertion wasDerivedFrom befree-20140225 NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_assertion wasGeneratedBy ECO_0000203 NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP813126.RA4NZINJTa2G-B1sotVxL6Vj_Z2R2940rie6bjZKpnaqk130_provenance.