@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI> .
@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:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_head {
  this: np:hasAssertion dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion;
    np:hasProvenance dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_provenance;
    np:hasPublicationInfo dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion a np:Assertion .
  
  dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_provenance a np:Provenance .
  
  dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion {
  miriam-gene:5308 a ncit:C16612 .
  
  lld:C3495489 a ncit:C7057 .
  
  dgn-gda:DGNeda8681fd784e854204c9703e89563be sio:SIO_000628 miriam-gene:5308, lld:C3495489;
    a sio:SIO_001121 .
}

dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_provenance {
  dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion dcterms:description
      "[Given the lack of any novel genes near either breakpoint, changes in potential regulatory elements may be the best model to explain the loss of PITX2 expression in these patients and hence the Rieger's syndrome phenotype.]. 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:14991915;
    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:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:25+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" .
}