@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc> .
@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:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_head {
  this: np:hasAssertion dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_assertion;
    np:hasProvenance dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_provenance;
    np:hasPublicationInfo dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_assertion a np:Assertion .
  
  dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_provenance a np:Provenance .
  
  dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_assertion {
  miriam-gene:952 a ncit:C16612 .
  
  lld:C0729233 a ncit:C7057 .
  
  dgn-gda:DGNe6ca7e22307d86489ff1aa6177bbd010 sio:SIO_000628 miriam-gene:952, lld:C0729233;
    a sio:SIO_001121 .
}

dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_provenance {
  dgn-np:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_assertion dcterms:description
      "[Radiographs demonstrated a distinct spondyloepiphyseal dysplasia in which the most striking changes were confined to the thoracic spine (flattening and collapse in T7, T8 and T10 vertebral bodies) and to the femoral capital epiphyses (irregularities and fragmentation).]. 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:1456283;
    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:NP885263.RAuqHuO0wI4rV65OAT22OUeD5eWxQ8q08LU_7OAU30Hhc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}