@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss> .
@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:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_head {
  this: np:hasAssertion dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion;
    np:hasProvenance dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_provenance;
    np:hasPublicationInfo dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion a np:Assertion .
  
  dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_provenance a np:Provenance .
  
  dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion {
  miriam-gene:9289 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGNda7ac865df1beafdcfa296dbf90e4074 sio:SIO_000628 miriam-gene:9289, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_provenance {
  dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion dcterms:description
      "[Functional studies of the GPR56 gene product will yield insights not only into the causes of polymicrogyria but also into the mechanisms of normal cortical development and the regional patterning of the cerebral cortex.]. 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:15863665;
    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:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:22+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" .
}