@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_head {
  this: np:hasAssertion dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion;
    np:hasProvenance dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_provenance;
    np:hasPublicationInfo dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion a np:Assertion .
  
  dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_provenance a np:Provenance .
  
  dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion {
  miriam-gene:2324 a ncit:C16612 .
  
  lld:C1704423 a ncit:C7057 .
  
  dgn-gda:DGN9d9322dd5062565d086b088a8e4f7bce sio:SIO_000628 miriam-gene:2324, lld:C1704423;
    a sio:SIO_001121 .
}

dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_provenance {
  dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion dcterms:description
      "[The clinical presentation, similar to Milroy disease, indicates an overlapping of the external phenotype of both diseases, suggesting that genetic analysis of VEGFC would be useful in diagnosing patients that present with Milroy features but have no mutation in VEGFR-3.]. 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:24744435;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:37+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}