@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_head {
  this: np:hasAssertion dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_assertion;
    np:hasProvenance dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_provenance;
    np:hasPublicationInfo dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_assertion a np:Assertion .
  
  dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_provenance a np:Provenance .
  
  dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0086543 a ncit:C7057 .
  
  dgn-gda:DGN12a16aa000a4284dff4c81380c0b6dfd sio:SIO_000628 miriam-gene:2952, lld:C0086543;
    a sio:SIO_001122 .
}

dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_provenance {
  dgn-np:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_assertion dcterms:description
      "[An association was observed between GSTT1 CNV and ARC in a Han Chinese population. The GSTT1 CNV is most closely associated with cortical cataract risk. The loss of at least one GSTT1 allele increases the risk of cortical cataract, whereas gain in GSTT1 c]. 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:20335620;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP168267.RA9a1KPjcwCQ6WHEUlQWXPi-MAC5_L4VRyK65AOVswO0E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:03+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}