@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI> .
@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:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_head {
  this: np:hasAssertion dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_assertion;
    np:hasProvenance dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_provenance;
    np:hasPublicationInfo dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_assertion a np:Assertion .
  
  dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_provenance a np:Provenance .
  
  dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_assertion {
  miriam-gene:1592 a ncit:C16612 .
  
  lld:C0010278 a ncit:C7057 .
  
  dgn-gda:DGNc11a6e282dd535c848ca0f70bc7f7932 sio:SIO_000628 miriam-gene:1592, lld:C0010278;
    a sio:SIO_001121 .
}

dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_provenance {
  dgn-np:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_assertion dcterms:description
      "[Analyses of murine embryos exposed to a chemical inhibitor of Cyp26 enzymes and zebrafish lines with mutations in cyp26b1 suggest that the endochondral bone fusions are due to unrestricted chondrogenesis at the presumptive sites of joint formation within cartilaginous templates, whereas craniosynostosis is induced by a defect in osteoblastic differentiation.]. 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:22019272;
    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:NP748167.RATA5qahkJ2m8o-9JvwjcWtw9WwsL4qWNw6DIOuy8qHSI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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" .
}