@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo> .
@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:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_head {
  this: np:hasAssertion dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_assertion;
    np:hasProvenance dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_provenance;
    np:hasPublicationInfo dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_assertion a np:Assertion .
  
  dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_provenance a np:Provenance .
  
  dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_assertion {
  miriam-gene:3557 a ncit:C16612 .
  
  lld:C0277554 a ncit:C7057 .
  
  dgn-gda:DGN1b248148503064845f2dfa25a163d86f sio:SIO_000628 miriam-gene:3557, lld:C0277554;
    a sio:SIO_001121 .
}

dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_provenance {
  dgn-np:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_assertion dcterms:description
      "[While in patients with chronic lymphocytic leukemia (CLL), hairy cell leukemia (HCL), multiple myeloma (MM) and related disorders, primary acute myeloid leukemia (AML), chronic myeloid leukemia (CML), and Hodgkin's disease (HD), the allelic distribution of IL-1RN was comparable to that seen in healthy control subjects, in a small group of patients with secondary AML the frequency of the IL-1RN*4 allele appeared to be significantly increased.]. 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:9384710;
    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:NP202622.RAha8h2QDxfaB-B7qUMoL1qXWfomh7dHyIUEmQ6pKcdHo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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" .
}