@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k> .
@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:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_head {
  this: np:hasAssertion dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_assertion;
    np:hasProvenance dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_provenance;
    np:hasPublicationInfo dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_assertion a np:Assertion .
  
  dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_provenance a np:Provenance .
  
  dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_assertion {
  miriam-gene:8910 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGNaff1534c86e1970e5394fb27787e593e sio:SIO_000628 miriam-gene:8910, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_provenance {
  dgn-np:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_assertion dcterms:description
      "[In SGCE mutation carriers, we observed significant hyperresponsiveness in contralateral inferior parietal cortical areas, ipsilateral premotor and primary somatosensory cortex, and ipsilateral cerebellum during the motor task compared with healthy control subjects.]. 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:20385914;
    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:NP539028.RABpnrnjRvPbVZkjMYavzLI4m29WtCQPWZ85w_t6eKH7k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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" .
}