@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg> .
@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:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_head {
  this: np:hasAssertion dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_assertion;
    np:hasProvenance dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_provenance;
    np:hasPublicationInfo dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_assertion a np:Assertion .
  
  dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_provenance a np:Provenance .
  
  dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_assertion {
  miriam-gene:4060 a ncit:C16612 .
  
  lld:C0154778 a ncit:C7057 .
  
  dgn-gda:DGN31f31af82259526fe11122ddc2ce6f6e sio:SIO_000628 miriam-gene:4060, lld:C0154778;
    a sio:SIO_001122 .
}

dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_provenance {
  dgn-np:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_assertion dcterms:description
      "[Genetic variation in the regulatory domains of the lumican gene, where both rs3759223 and rs3741834 are located, are associated with high myopia susceptibility among the Han Chinese, making this region worthy of further investigation.]. 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:19616852;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP70176.RAReFXy63vcKbTIedr_cWu-_fBmxiTW995Oz0x1qI-Csg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:34+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" .
}