@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg> .
@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:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_head {
  this: np:hasAssertion dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_assertion ;
    np:hasProvenance dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_provenance ;
    np:hasPublicationInfo dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_assertion a np:Assertion .
  dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_provenance a np:Provenance .
  dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_assertion {
  miriam-gene:7141 a ncit:C16612 .
  lld:C0035435 a ncit:C7057 .
  dgn-gda:DGN3bf27c73ab3cec09ae81407f5bf829c4 sio:SIO_000628 miriam-gene:7141 , lld:C0035435 ;
    a sio:SIO_001121 .
}
dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_provenance {
  dgn-np:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_assertion dcterms:description "[Since all of these functions are of potential importance in the induction or maintenance or both of autoimmune disease, samples from the Arthritis and Rheumatism Council's repository of multicase rheumatoid arthritis families were typed for a dinucleotide repeat in the NRAMP1 promoter region and four other 2q34 (TNP1) or 2q35 (IL8R, VIL1, DES) marker genes.]. 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:8863160 ;
    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:NP437262.RAdWbsCLilPX_0NNBt-E-cthRLun553FJtMpMcPdd1QXg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:19+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" .
}