@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI> .
@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:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_head {
  this: np:hasAssertion dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_assertion ;
    np:hasProvenance dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_provenance ;
    np:hasPublicationInfo dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_assertion a np:Assertion .
  dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_provenance a np:Provenance .
  dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_assertion {
  miriam-gene:144100 a ncit:C16612 .
  lld:C0017606 a ncit:C7057 .
  dgn-gda:DGNb9e373417744282f231cd3e698b024ed sio:SIO_000628 miriam-gene:144100 , lld:C0017606 ;
    a sio:SIO_001121 .
}
dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_provenance {
  dgn-np:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_assertion dcterms:description "[Three loci defined by single nucleotide polymorphisms (SNPs) rs11024102 in PLEKHA7, rs3753841 in COL11A1, and rs1015213 between the PCMTD1 and ST18 genes, recently have been associated with primary angle closure glaucoma (PACG).]. 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:23847314 ;
    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:NP388912.RAeq3qGD-5ZP-nIfcdYeiShCd3TFHv8JZufqgZpzGyIQI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}