@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0> .
@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:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_head {
  this: np:hasAssertion dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_assertion;
    np:hasProvenance dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_provenance;
    np:hasPublicationInfo dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_assertion a np:Assertion .
  
  dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_provenance a np:Provenance .
  
  dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_assertion {
  miriam-gene:11330 a ncit:C16612 .
  
  lld:C0149521 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_provenance {
  dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_assertion dcterms:description
      "[The authors sequenced all eight exons and flanking regions in CTRC in 584 CP patients (497 TCP, 87 idiopathic CP) and 598 normal subjects and analysed the significance of association using χ(2) test.]. 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:22580415;
    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:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+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" .
}