@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE> .
@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:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_head {
   this: np:hasAssertion dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_assertion ;
    np:hasProvenance dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_provenance ;
    np:hasPublicationInfo dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_assertion a np:Assertion .
  dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_provenance a np:Provenance .
  dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_assertion {
   miriam-gene:2722 a ncit:C16612 .
  lld:C0339573 a ncit:C7057 .
  dgn-gda:DGN6c88409f3dc2378d8e39c4d5bbd61192 sio:SIO_000628 miriam-gene:2722 , lld:C0339573 ;
    a sio:SIO_001121 .
}
dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_provenance {
   dgn-np:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_assertion dcterms:description "[The aim of the present study was to examine the genetic background of primary open angle glaucoma (POAG) in the Finnish population by analyzing previously reported candidate loci GLC1B on 2cen-q13, GLCIC on 3q21-q24, GLC1D on 8q23, GLC1F on 7q35-q36, as well as other candidate regions on chromosomes 2p14, 2q33-34, 10p12-13, 14q11, 14q21-22, 17p13, 17q25, and 19q12-14.]. 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:15073581 ;
    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:NP636153.RAEhUCxnvc_W3ar2E6xYrZDH4txHUpkjvxlY5c9hhiMlE130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:23+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" .
}