Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- gad-20150221 importedOn "2015-02-21" NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_assertion wasGeneratedBy ECO_0000203 NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_assertion wasDerivedFrom gad-20150221 NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_assertion SIO_000772 14693734 NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_assertion evidence source_evidence_literature NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.
- NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_assertion description "[Moreover, the occurrence rate of combinations and estimated haplotypes containing these HLA alleles was strikingly different in meningioma patients compared with controls: significantly increased for the haplotypes HLA-A*02:DRB1*04 (P = 0.02, relative risk = 2.5) and HLA-A*02:DRB1*04:DQB1*0302,DQB1*05 (P = 0.03, RR = 7.5), and significantly decreased for the haplotype HLA-A*01:B*08:DRB1*03 (P = 0.01, relative risk = 0.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83202.RAp2Fd5OtkylH7m-dOHSzX1f-mIAm1jNuraLRtEAHJV5Y130_provenance.