@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A> .
@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:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_head {
  this: np:hasAssertion dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_assertion;
    np:hasProvenance dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_provenance;
    np:hasPublicationInfo dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_assertion a np:Assertion .
  
  dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_provenance a np:Provenance .
  
  dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0521707 a ncit:C7057 .
  
  dgn-gda:DGN41096df6955f58844dc01b8560495f3f sio:SIO_000628 miriam-gene:2944, lld:C0521707;
    a sio:SIO_001121 .
}

dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_provenance {
  dgn-np:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_assertion dcterms:description
      "[The frequency of GSTM1 positive individuals was significantly higher in MT cataracts followed by NC, CC and PSC types with corresponding decrease in the GSTM1 null genotypes as compared to controls.]. 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:22446016;
    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:NP179468.RA53aMjvhU2DmRmCA3fdN4pr5bYtm98DdYdk7Ppxtem4A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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" .
}