Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_assertion description "[We conclude that specific MHC II pocket amino acid signatures determine susceptibility to HT and EAT by causing structural changes in peptide-binding pockets that may influence peptide binding, selectivity, and presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_assertion evidence source_evidence_literature NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_assertion SIO_000772 18779568 NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_assertion wasDerivedFrom befree-20140225 NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_assertion wasGeneratedBy ECO_0000203 NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449754.RAHvDxKi80hT2PJrPkUbqViGCFw2YQ-Fso6aD-DVUcaLE130_provenance.