Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_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." NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_assertion evidence source_evidence_literature NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_assertion SIO_000772 7483776 NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_assertion wasDerivedFrom befree-20150227 NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_assertion wasGeneratedBy ECO_0000203 NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP456038.RAk-QsCJBC32cJJNy_wVhu4jJEeLyy2TFhM6iPNoe-fgE130_provenance.