@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw> .
@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/v4.0.0/void/> .

dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_head {
  this: np:hasAssertion dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_assertion;
    np:hasProvenance dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_provenance;
    np:hasPublicationInfo dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_assertion a np:Assertion .
  
  dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_provenance a np:Provenance .
  
  dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_assertion {
  miriam-gene:4297 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN3e2ec3bdd794ed5583ff92e1f07666af sio:SIO_000628 miriam-gene:4297, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_provenance {
  dgn-np:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_assertion dcterms:description
      "[The results support the concept that CLL/MLL is a condition of multiple aetiologies with evidence for genetic predisposition through an excess of family cases, immune perturbation demonstrated by excessive previous skin diseases and phenylbutazone use, and viral involvement shown by links with infectious diseases and multiple sclerosis.]. 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:3304389;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1301292.RAhRvPkWquxhLkhaIzIRSHucfuWBY2ZysC_ytLNDEY_Cw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:35+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}