@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw> .
@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:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_head {
  this: np:hasAssertion dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_assertion ;
    np:hasProvenance dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_provenance ;
    np:hasPublicationInfo dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_assertion a np:Assertion .
  dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_provenance a np:Provenance .
  dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_assertion {
  miriam-gene:4340 a ncit:C16612 .
  lld:C0162309 a ncit:C7057 .
  dgn-gda:DGNa4bfda36b4c5f3aa1a0eab74375ac4a0 sio:SIO_000628 miriam-gene:4340 , lld:C0162309 ;
    a sio:SIO_001121 .
}
dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_provenance {
  dgn-np:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_assertion dcterms:description "[In the present study, we investigated the possible association of (1) a naturally occurring variable number tandem repeat (vntr) polymorphism (C allele) in the 3' flanking region of the interleukin-6 gene (IL-6), previously demonstrated to modify the course of Alzheimer's disease, systemic lupus erythematodes and Multiple Sclerosis (MS), (2) a tetranucleotide repeat polymorphism (TAAA)(n) in the 3' flanking region of the MOG gene and (3) HLA class II alleles with adult clinical phenotypes and serum antibody responses to MOG in 70 adult X-ALD patients.]. 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:12576235 ;
    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:NP929007.RA4-K-G2X_8rOQzCcjfv3cLORftvx67sFhVpcelnmo8iw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}