@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s> .
@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:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_head {
  this: np:hasAssertion dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion;
    np:hasProvenance dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_provenance;
    np:hasPublicationInfo dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion a np:Assertion .
  
  dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_provenance a np:Provenance .
  
  dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion {
  miriam-gene:2324 a ncit:C16612 .
  
  lld:C0020305 a ncit:C7057 .
  
  dgn-gda:DGNc346c4fc2e3fbd6efaf4855fdb353c33 sio:SIO_000628 miriam-gene:2324, lld:C0020305;
    a sio:SIO_001121 .
}

dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_provenance {
  dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion dcterms:description
      "[Because VEGFR3 mutation can cause generalized lymphatic dysfunction and can thus result in hydrops fetalis, VEGFR3 screening should be added to the investigation of cases of hydrops fetalis of an unknown etiology.]. 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:16965327;
    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:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:23+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" .
}