@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA> .
@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:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_head {
  this: np:hasAssertion dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_assertion;
    np:hasProvenance dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_provenance;
    np:hasPublicationInfo dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_assertion a np:Assertion .
  
  dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_provenance a np:Provenance .
  
  dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_assertion {
  miriam-gene:27086 a ncit:C16612 .
  
  lld:C0023015 a ncit:C7057 .
  
  dgn-gda:DGNadda27b9a862dbb7e965b7044a1207d4 sio:SIO_000628 miriam-gene:27086, lld:C0023015;
    a sio:SIO_001121 .
}

dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_provenance {
  dgn-np:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_assertion dcterms:description
      "[FOXP2 and its closest homolog, FOXP1, are coexpressed in brain regions that are important for language and cooperatively regulate developmental processes, raising the possibility that FOXP1 may also be involved in developmental conditions that are associated with language impairment.]. 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:20950788;
    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:NP853194.RAFg9XTyfGkR27gu0C_pOXLK5ih9_M96ighHLx0Nm-sEA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:42+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" .
}