@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k> .
@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:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_head {
  this: np:hasAssertion dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_assertion;
    np:hasProvenance dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_provenance;
    np:hasPublicationInfo dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_assertion a np:Assertion .
  
  dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_provenance a np:Provenance .
  
  dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_assertion {
  miriam-gene:2324 a ncit:C16612 .
  
  lld:C0024236 a ncit:C7057 .
  
  dgn-gda:DGN0be158c743f52b729d30566b847415ff sio:SIO_000628 miriam-gene:2324, lld:C0024236;
    a sio:SIO_001121 .
}

dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_provenance {
  dgn-np:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_assertion dcterms:description
      "[The prenatal nuchal lymphedema associated with this deletion syndrome my be related to the deletion of the FLT4 gene causing autosomal dominant primary lymphedema and contributes to the differential diagnosis of increased fetal nuchal translucency.]. 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:12900893;
    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:NP530543.RAbNtZwbQMKdroiPjrf3EzRrNvRIowkAvjY1cEjSQ7H0k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:20+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" .
}