@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac> .
@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 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:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_head {
  this: np:hasAssertion dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_assertion;
    np:hasProvenance dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_provenance;
    np:hasPublicationInfo dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_assertion a np:Assertion .
  
  dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_provenance a np:Provenance .
  
  dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN435e88337f0d46328515d9880e8e470e sio:SIO_000628 miriam-gene:7421, lld:C0023418;
    a sio:SIO_001122 .
}

dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_provenance {
  dgn-np:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_assertion dct:description
      "[Distribution of Fokl and Bsml genotype is in accordance with data for Caucasian population. Assessed data suggest that children treated for leukemia are carriers of alleles which negatively influence on skeletal system.]. 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:20568398;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP59107.RA9fJyyk-InM2frBQlKIPvfOlZ42OGE0uKuesCrfzTpac130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}