Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_assertion description "[Specifically, there was a significant difference in the HLA-DQA1*0102 allele frequencies between AAA cases (67/322 alleles, 20.8%) and controls (44/356 alleles, 12.4%) in Belgian males (empirical p = 0.019, asymptotic p = 0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_assertion evidence source_evidence_literature NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_assertion SIO_000772 16879749 NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_assertion wasDerivedFrom befree-20140225 NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_assertion wasGeneratedBy ECO_0000203 NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP808822.RAIah_M3c_d8Tr-rzYURmkmd5GV3rvx2bcrK1JWOMD2K4130_provenance.