@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg> .
@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:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_head {
  this: np:hasAssertion dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion;
    np:hasProvenance dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_provenance;
    np:hasPublicationInfo dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion a np:Assertion .
  
  dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_provenance a np:Provenance .
  
  dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion {
  miriam-gene:1415 a ncit:C16612 .
  
  lld:C0086543 a ncit:C7057 .
  
  dgn-gda:DGNdfe26fa2a5c7430d55c0cdf0f8191d8a sio:SIO_000628 miriam-gene:1415, lld:C0086543;
    a sio:SIO_001121 .
}

dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_provenance {
  dgn-np:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_assertion dcterms:description
      "[Blood was taken from the proband and his parents, genomic DNA was isolated and some candidate genes for cataract (CRYAA, CRYBB2, GJA8) or macular hypoplasia (OA1, P) or both (PAX6) were analyzed.]. 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:16453125;
    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:NP560732.RAdLVGWYybVhLVeAQHQqDQ-Qd2kYbaF4gRBbAHoV-Yrbg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:38+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" .
}