@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE> .
@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:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_head {
  this: np:hasAssertion dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion;
    np:hasProvenance dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_provenance;
    np:hasPublicationInfo dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion a np:Assertion .
  
  dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_provenance a np:Provenance .
  
  dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN346630b5ff9c874a231e3073c5474dd7 sio:SIO_000628 miriam-gene:183, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_provenance {
  dgn-np:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_assertion dcterms:description
      "[After informed consent was obtained, 63 patients (21 stroke subjects and 42 nonstroke control subjects matched according to age and sex) with SCD followed at local pediatric hematology clinics were genotyped to test the association of specific GT-repeat alleles of the AGT gene and occurrence of stroke.]. 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:11754397;
    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:NP573510.RAzWI3TR7YmVH3rAzcnQbNErdTP48ADOEB69ueAwwywuE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:45+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" .
}