@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM> .
@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:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_head {
  this: np:hasAssertion dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_assertion;
    np:hasProvenance dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_provenance;
    np:hasPublicationInfo dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_assertion a np:Assertion .
  
  dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_provenance a np:Provenance .
  
  dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_assertion {
  miriam-gene:2303 a ncit:C16612 .
  
  lld:C0265345 a ncit:C7057 .
  
  dgn-gda:DGN8041966f553eab5babc417f7777dfc66 sio:SIO_000628 miriam-gene:2303, lld:C0265345;
    a sio:SIO_001121 .
}

dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_provenance {
  dgn-np:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_assertion dcterms:description
      "[Seven sporadic SEDAC subjects had no FOXC2 mutations, no symptoms of LDS, and showed differing clinical characteristics from those who had FOXC2 mutations, suggesting that other gene(s) besides FOXC2 are likely to be involved in SEDAC.]. 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:24278289;
    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:NP404758.RA8PeOi6c3ncDkT6ptOd9K-eG-gWSpdY5Tz97Pc1a3zHM130_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" .
}