@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ> .
@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:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_head {
  this: np:hasAssertion dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_assertion;
    np:hasProvenance dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_provenance;
    np:hasPublicationInfo dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_assertion a np:Assertion .
  
  dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_provenance a np:Provenance .
  
  dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_assertion {
  miriam-gene:2728 a ncit:C16612 .
  
  lld:C0020302 a ncit:C7057 .
  
  dgn-gda:DGN8eec62775de8a246e078b11e21e80ac6 sio:SIO_000628 miriam-gene:2728, lld:C0020302;
    a sio:SIO_001121 .
}

dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_provenance {
  dgn-np:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_assertion dcterms:description
      "[The autosomal recessive form of primary congenital glaucoma (gene symbol GLC3) has been recently mapped to two different loci, GLC3A (at 2p21), and GLC3B (at 1p36), respectively, on families of Turkish and Saudi Arabian provenance.]. 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:9463798;
    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:NP175609.RAf-cL27vum3_gmGGxavdt3aHhhAFpJ6Cupw74qKqv7kQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}