@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc> .
@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:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_head {
  this: np:hasAssertion dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_assertion ;
    np:hasProvenance dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_provenance ;
    np:hasPublicationInfo dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_assertion a np:Assertion .
  dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_provenance a np:Provenance .
  dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_assertion {
  miriam-gene:1296 a ncit:C16612 .
  lld:C0017612 a ncit:C7057 .
  dgn-gda:DGN604380636470633206ea06d7366a108c sio:SIO_000628 miriam-gene:1296 , lld:C0017612 ;
    a sio:SIO_001122 .
}
dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_provenance {
  dgn-np:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_assertion dcterms:description "[In this study we have identified COL8A2 missense changes in a group of Caucasian patients with very thin CCT and advanced POAG. These results suggest that DNA sequence variants in the COL8A2 gene may be associated with thin corneas in some glaucoma patients. Further study of COL8A2 variants in other patient populations, especially those with thinner CCT such as African-Americans would provide further support for a role of COL8A2 in corneal thickness and in glaucoma.]. 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:21139683 ;
    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:NP89374.RADLrXlYA9OuUxr-Z43MSN_d_vkNCr1aQoa6mQQUUoxAc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:44+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" .
}