@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c> .
@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:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_head {
  this: np:hasAssertion dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_assertion;
    np:hasProvenance dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_provenance;
    np:hasPublicationInfo dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_assertion a np:Assertion .
  
  dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_provenance a np:Provenance .
  
  dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_assertion {
  miriam-gene:30813 a ncit:C16612 .
  
  lld:C0339284 a ncit:C7057 .
  
  dgn-gda:DGNe850118d0a8f57b3701d94fbbe6fd140 sio:SIO_000628 miriam-gene:30813, lld:C0339284;
    a sio:SIO_001121 .
}

dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_provenance {
  dgn-np:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_assertion dcterms:description
      "[Therefore, although we report a number of novel polymorphisms in the VSX1 and ID1 genes, the failure to identify any sequence variants that sort with the disease phenotype suggests that other genetic factors are involved in PPCD.]. 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:15725882;
    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:NP681678.RAC68D_05YR4PQyeK1TAY-OW_45gjW7JJvgqBWbcO044c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:51+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" .
}