@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k> .
@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:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_head {
  this: np:hasAssertion dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_assertion;
    np:hasProvenance dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_provenance;
    np:hasPublicationInfo dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_assertion a np:Assertion .
  
  dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_provenance a np:Provenance .
  
  dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_assertion {
  miriam-gene:2300 a ncit:C16612 .
  
  lld:C0152101 a ncit:C7057 .
  
  dgn-gda:DGNa9d214d490d8e3a301c3d38f9739006b sio:SIO_000628 miriam-gene:2300, lld:C0152101;
    a sio:SIO_001121 .
}

dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_provenance {
  dgn-np:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_assertion dcterms:description
      "[In contrast to the association of point mutations in FOXF1 with bowel malrotation, microdeletions of FOXF1 were associated with hypoplastic left heart syndrome and gastrointestinal atresias, probably due to haploinsufficiency for the neighboring FOXC2 and FOXL1 genes.]. 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:19500772;
    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:NP231124.RABFn95fmky8bQ1bWl_jyTtkGfcsL3t-OJreR0zomi5-k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}