@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE> .
@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:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_head {
  this: np:hasAssertion dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_assertion;
    np:hasProvenance dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_provenance;
    np:hasPublicationInfo dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_assertion a np:Assertion .
  
  dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_provenance a np:Provenance .
  
  dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C1261473 a ncit:C7057 .
  
  dgn-gda:DGN337cac5de86c926215985b68d11f1075 sio:SIO_000628 miriam-gene:2099, lld:C1261473;
    a sio:SIO_001121 .
}

dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_provenance {
  dgn-np:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_assertion dcterms:description
      "[For the molecular analysis, genetic polymorphisms of the VDR (Fok I, Apa I, and TaqI), ER (Pvu II and XbaI), and COLIalpha1 (Msc I) genes were characterized in 72 osteosarcoma and 53 Ewing sarcomas and in a group of 143 healthy matched children.]. 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:14528100;
    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:NP859102.RAyteiP_24OFnrNLZ_m8_vn1-YOCoHm387vEFsOzgpcdE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:45+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" .
}