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- source_evidence_literature type ECO_0000212 NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_assertion description "[Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_assertion evidence source_evidence_literature NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_assertion SIO_000772 8402893 NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_assertion wasDerivedFrom befree-20150227 NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_assertion wasGeneratedBy ECO_0000203 NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP556063.RAnH_T3s3gaONaNzE44NjosPWwzPESReMT84Xx4roH7JA130_provenance.