@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ> .
@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:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_head {
  this: np:hasAssertion dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion;
    np:hasProvenance dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_provenance;
    np:hasPublicationInfo dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion a np:Assertion .
  
  dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_provenance a np:Provenance .
  
  dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion {
  miriam-gene:2153 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN2cd9df828b31e6af9ac70a37d2cdf9cd sio:SIO_000628 miriam-gene:2153, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_provenance {
  dgn-np:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_assertion dcterms:description
      "[This study shows that for some genes, further studies are unnecessary, whereas for others, no more enrollments are needed. The impact of certain genotypes must be examined in relation to other established risk factors and potentially new therapeutic strategies.]. 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:11397354;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP44449.RASIO3RPc6vZFoSjC4M0aFkpFV730EUUuusigUfyIdDRQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}