@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570> .
@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:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_head {
  this: np:hasAssertion dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion;
    np:hasProvenance dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_provenance;
    np:hasPublicationInfo dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion a np:Assertion .
  
  dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_provenance a np:Provenance .
  
  dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion {
  miriam-gene:3566 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNd475ec0a292376c81af3a45e95ffdcaf sio:SIO_000628 miriam-gene:3566, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_provenance {
  dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion dcterms:description
      "[By genotyping two promoter and eight coding IL4R SNPs and identifying haplotypes (complex alleles) in the MS families, stratified for HLA genotype, we have observed evidence of the association of the IL4R gene to MS.]. 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:14712310;
    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:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}