@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU> .
@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/v4.0.0/void/> .
dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_head {
   this: np:hasAssertion dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_assertion ;
    np:hasProvenance dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_provenance ;
    np:hasPublicationInfo dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_assertion a np:Assertion .
  dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_provenance a np:Provenance .
  dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_assertion {
   miriam-gene:93986 a ncit:C16612 .
  lld:C0023015 a ncit:C7057 .
  dgn-gda:DGNa9ab038b5d3ce302aa78c627ad429523 sio:SIO_000628 miriam-gene:93986 , lld:C0023015 ;
    a sio:SIO_001121 .
}
dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_provenance {
   dgn-np:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_assertion dcterms:description "[Because of the chromosomal location of FOXP2 (7q31) and the putative implication of the 7q31 region both in autistic and in language disorders (a feature of AD), it has been hypothesized that FOXP2 may be implicated in the pathophysiology of AD.]. 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:12655497 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP388444.RAleU7prFQh3VJHGknUFgB7D9V8V6cnWpXbxr8dHrxLVU130_publicationInfo {
   this: dcterms:created "2016-05-13T12:44:41+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}