@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_head {
  this: np:hasAssertion dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_assertion ;
    np:hasProvenance dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_provenance ;
    np:hasPublicationInfo dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_assertion a np:Assertion .
  dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_provenance a np:Provenance .
  dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_assertion {
  miriam-gene:1810 a ncit:C16612 .
  lld:C0270814 a ncit:C7057 .
  dgn-gda:DGNb03a9cbd3b03e5c3782f011b8edbf198 sio:SIO_000628 miriam-gene:1810 , lld:C0270814 ;
    a sio:SIO_001121 .
}
dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_provenance {
  dgn-np:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_assertion dcterms:description "[The problem of understanding the meaning of the association of susceptibility with diverse MHC alleles such as DR4 (Dw4 and Dw14), DR1, and DRw10 is approached by detailed biochemical analysis that led to the identification of common stretches of amino acid sequence, presumably encoding conformationally equivalent structures.]. 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:3142068 ;
    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:NP623927.RArvRat-43wf1PP-FxrHExcy0IdoIbPFlgbzQjyugKBSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:16+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}