@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo> .
@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:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_head {
  this: np:hasAssertion dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion;
    np:hasProvenance dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_provenance;
    np:hasPublicationInfo dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion a np:Assertion .
  
  dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_provenance a np:Provenance .
  
  dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion {
  miriam-gene:1594 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGNb6a047342f1e3986805a30784445515e sio:SIO_000628 miriam-gene:1594, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_provenance {
  dgn-np:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_assertion dcterms:description
      "[The purpose of this study is to ascertain whether VDR genotype which is involved in the risk for many cancers including multiple myeloma is also correlated with cancers in patients with Gaucher disease.]. 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:20920864;
    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:NP292557.RAKHr6Qfdw-wtPgi2UiSi8ibkaL_yv7IkkCe9bi31eUmo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:46+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" .
}