@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks> .
@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:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_head {
  this: np:hasAssertion dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion;
    np:hasProvenance dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_provenance;
    np:hasPublicationInfo dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion a np:Assertion .
  
  dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_provenance a np:Provenance .
  
  dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion {
  miriam-gene:7439 a ncit:C16612 .
  
  lld:C0035309 a ncit:C7057 .
  
  dgn-gda:DGNd05d53d703036a5aa39ec354dbb5991a sio:SIO_000628 miriam-gene:7439, lld:C0035309;
    a sio:SIO_001121 .
}

dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_provenance {
  dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion dcterms:description
      "[These data confirm the involvement of the VMD2 gene in Best macular dystrophy onset, even in sporadic cases of the disease, pointing out the relevance of molecular analysis in the diagnosis of this degenerative retinal disease.]. 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:10682987;
    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:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:24+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" .
}