@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_head { this: np:hasAssertion dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_assertion; np:hasProvenance dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_provenance; np:hasPublicationInfo dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_publicationInfo; a np:Nanopublication . dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_assertion a np:Assertion . dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_provenance a np:Provenance . dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_publicationInfo a np:PublicationInfo . } dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_assertion { miriam-gene:3123 a ncit:C16612 . lld:C0854359 a ncit:C7057 . dgn-gda:DGN9c02251bfc7d403b22fb739303b26b5d sio:SIO_000628 miriam-gene:3123, lld:C0854359; a sio:SIO_001121 . } dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_provenance { dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_assertion dcterms:description "[We analyzed structural motifs of peptides bound to HLA-DR4 (DRB1*0405 and DRB1*0406) and DR9 (DRB1*0901) and found that: (a) AxxBxC motif where A, B, and C are hydrophobic, hydrophobic, and neutral, respectively, is important for binding to DR4; (b) Gln (Q) or Ser at position C allow high-affinity binding specific to DRB1*0406 which is strongly associated with insulin autoimmune syndrome; (c) among human insulin-derived peptide fragments, the TSICSLYQLE of the human insulin alpha chain, which is exposed only under reducing conditions, has the highest affinity specific to DRB1*0406 by binding with the IxxLxQ motif; (d) a short-term human insulin-specific T cell line recognizes a peptide fragment containing the IxxLxQ motif as a major T cell epitope; and (e) in the AxxB motif, where A and B need to be hydrophobic for binding to DR9, neutral Ser is exceptionally allowed at position B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:9119530; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP225428.RAnLbKy_EWDBMzgwW6QapaXLbWYfo4qzZhmfPTlpFYz0A130_publicationInfo { this: dcterms:created "2014-10-02T12:34:05+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }