Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_assertion> ?p ?o ?g. }
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- NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_assertion type Assertion NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_head.
- NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_assertion wasGeneratedBy ECO_0000203 NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_provenance.
- NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_assertion wasDerivedFrom gad-20150221 NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_provenance.
- NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_assertion SIO_000772 20622878 NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_provenance.
- NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_assertion evidence source_evidence_literature NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_provenance.
- NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_assertion description "[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181058.RAYX5iacxsEokPSx1_hnKJQMSpp9_eloYDztXSg7e1yzE130_provenance.