@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo> .
@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:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_head {
  this: np:hasAssertion dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_assertion ;
    np:hasProvenance dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_provenance ;
    np:hasPublicationInfo dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_assertion a np:Assertion .
  dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_provenance a np:Provenance .
  dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_assertion {
  miriam-gene:8896 a ncit:C16612 .
  lld:C0014072 a ncit:C7057 .
  dgn-gda:DGN99f0646b8d3401b94ef172510677853c sio:SIO_000628 miriam-gene:8896 , lld:C0014072 ;
    a sio:SIO_001121 .
}
dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_provenance {
  dgn-np:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_assertion dcterms:description "[We used high resolution quantitative trait loci (QTL) analysis in the 10th generation (G10) of an advanced intercross line (AIL) to resolve Eae23 into two QTLs that independently regulate EAE, namely Eae23a and Eae23b.]. 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:20856809 ;
    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:NP880506.RACKVc0c6Meg9bOPSWvWTrLBDevfpt-9pg9_TPY8BWaLo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:58+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> ;
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}