@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_head {
  this: np:hasAssertion dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_assertion ;
    np:hasProvenance dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_provenance ;
    np:hasPublicationInfo dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_assertion a np:Assertion .
  dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_provenance a np:Provenance .
  dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_assertion {
  miriam-gene:1234 a ncit:C16612 .
  lld:C0009324 a ncit:C7057 .
  dgn-gda:DGN9c665f43e2718006402a6b5afd4a42fd sio:SIO_000628 miriam-gene:1234 , lld:C0009324 ;
    a sio:SIO_001122 .
}
dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_provenance {
  dgn-np:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_assertion dcterms:description "[We did not find any significant correlation between a 32-bp deletion variant of CCR5 or a single nucleotide change A1902G (Gln576Arg) of IL4RA, and IBD phenotypes, with the exception that in the UC group homozygosity for the G1902 allele of IL4RA was less frequent (0.019 vs 0.049, P=0.038).]. 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:11378820 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP316807.RASIi3DZ1hbuqNSIp1qDXBvTFyuVJNW3nHX88mByucJMU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:42+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}