@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM> .
@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:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_head {
  this: np:hasAssertion dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion;
    np:hasProvenance dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_provenance;
    np:hasPublicationInfo dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion a np:Assertion .
  
  dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_provenance a np:Provenance .
  
  dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion {
  miriam-gene:55349 a ncit:C16612 .
  
  lld:C0152021 a ncit:C7057 .
  
  dgn-gda:DGNbd8117d66eae9aeb17681d341247631a sio:SIO_000628 miriam-gene:55349, lld:C0152021;
    a sio:SIO_001121 .
}

dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_provenance {
  dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion dcterms:description
      "[In the candidate region 12q13 of simple congenital heart disease(CHD), four single nucleotide polymorphisms(SNPs) in HOXC4 gene were chosen in order to investigate the distribution of SNP and haplotypes in simple CHD patients and normal people.]. 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:16215934;
    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:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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" .
}