@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs> .
@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:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_head {
  this: np:hasAssertion dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_assertion;
    np:hasProvenance dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_provenance;
    np:hasPublicationInfo dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_assertion a np:Assertion .
  
  dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_provenance a np:Provenance .
  
  dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_assertion {
  miriam-gene:100188864 a ncit:C16612 .
  
  lld:C0027708 a ncit:C7057 .
  
  dgn-gda:DGN9382f7367150db4d620539dbaa5481f5 sio:SIO_000628 miriam-gene:100188864,
      lld:C0027708;
    a sio:SIO_001121 .
}

dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_provenance {
  dgn-np:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_assertion dcterms:description
      "[Delineated features of this syndrome include visceromegaly, macrosomia, renal hamartomas, nephroblastomatosis, cryptorchidism in males, unusual facial appearance, polyhydramnios, fetal ascites, and Wilms tumor but do not include hemihypertrophy, omphalocele or umbilical abnormalities, aniridia, or other conditions known to be associated with Wilms tumor.]. 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:3010722;
    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:NP256881.RAA_8L_OW9u1ogXAf0Jyaj6yV0hldkPMuVR9Mu-RzAdAs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}