@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik> .
@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:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_head {
  this: np:hasAssertion dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_assertion;
    np:hasProvenance dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_provenance;
    np:hasPublicationInfo dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_assertion a np:Assertion .
  
  dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_provenance a np:Provenance .
  
  dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_assertion {
  miriam-gene:2703 a ncit:C16612 .
  
  lld:C0086543 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_provenance {
  dgn-np:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_assertion dcterms:description
      "[Mutation screening was performed in the cataract candidate genes coding for crystallins and connexin 50 by sequencing of polymerase chain reaction (PCR) products amplified from blood leukocyte DNA samples of eight family members.]. 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:18334966;
    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:NP303981.RA2YKCfbEzhzrML0Jwg0pkhpDMSUIrYdaQaGYJwlOEUik130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:54+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" .
}