@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_head {
  this: np:hasAssertion dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_assertion;
    np:hasProvenance dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_provenance;
    np:hasPublicationInfo dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_assertion a np:Assertion .
  
  dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_provenance a np:Provenance .
  
  dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_assertion {
  miriam-gene:2296 a ncit:C16612 .
  
  lld:C0017601 a ncit:C7057 .
  
  dgn-gda:DGNd80894901ba39d6249a1cedb2adfb069 sio:SIO_000628 miriam-gene:2296, lld:C0017601;
    a sio:SIO_001121 .
}

dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_provenance {
  dgn-np:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_assertion dcterms:description
      "[Thus, it is important to screen other glaucoma-associated loci and genes for involvement in congenital glaucoma in cases that are either negative or heterozygous for MYOC, CYP1B1, and FOXC1 mutations to have better insight into the disease pathogenesis.]. 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:23378721;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP404491.RAX25pRSwxicP-9wM4yczV2eS40bdWDTZjgwjaPbCYbAk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:35+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}