@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8> .
@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:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_head {
  this: np:hasAssertion dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_assertion;
    np:hasProvenance dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_provenance;
    np:hasPublicationInfo dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_assertion a np:Assertion .
  
  dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_provenance a np:Provenance .
  
  dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_assertion {
  miriam-gene:8521 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGNa3d2617dfd449152bf59b28ed4f3c432 sio:SIO_000628 miriam-gene:8521, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_provenance {
  dgn-np:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_assertion dcterms:description
      "[Our genome-wide association study identified SRBD1 and ELOVL5 as new susceptibility genes for NTG. Because SRBD1 and ELOVL5 are reportedly involved in the induction of cell growth inhibition or apoptosis, the regulation of SRBD1 and ELOVL5 cascades may play an important physiologic role in the risk of NTG development.]. 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:20363506;
    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:NP95089.RA-nKmHhNDfeZmD139qdJ7k5ye1BXsnsI_p3fACLA-OD8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
}