@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE> .
@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:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_head {
  this: np:hasAssertion dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_assertion;
    np:hasProvenance dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_provenance;
    np:hasPublicationInfo dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_assertion a np:Assertion .
  
  dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_provenance a np:Provenance .
  
  dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_assertion {
  miriam-gene:2303 a ncit:C16612 .
  
  lld:C0423848 a ncit:C7057 .
  
  dgn-gda:DGN22e64cda577565623faa53a048f681e6 sio:SIO_000628 miriam-gene:2303, lld:C0423848;
    a sio:SIO_001121 .
}

dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_provenance {
  dgn-np:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_assertion dcterms:description
      "[This Foxc2 mutant mouse thus provides an ideal model for exploring molecular mechanisms and physiologic events in mesenchymal differentiation associated with lymphatic growth and development and the clinical abnormalities seen in human LD syndrome.]. 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:12719382;
    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:NP404766.RAijt2TmVeXgoUNcMe8xwvFQB1ML7zZC0MEMZqFx4GxrE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:35+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" .
}