@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98> .
@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:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_head {
  this: np:hasAssertion dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion;
    np:hasProvenance dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_provenance;
    np:hasPublicationInfo dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion a np:Assertion .
  
  dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_provenance a np:Provenance .
  
  dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion {
  miriam-gene:7389 a ncit:C16612 .
  
  lld:C1297882 a ncit:C7057 .
  
  dgn-gda:DGNfed599aee78ce941dbe4d28eab091acf sio:SIO_000628 miriam-gene:7389, lld:C1297882;
    a sio:SIO_001121 .
}

dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_provenance {
  dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion dcterms:description
      "[PCR amplification of polymorphic loci mapping to 11p15.5 region documented partial trisomy of 11p15.5 due to paternal translocation in one, and segmental and mosaic segmental unipaternal disomy (UPD) in the second and third cases, respectively.]. 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:11807901;
    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:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}