@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw> .
@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:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_head {
  this: np:hasAssertion dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_assertion;
    np:hasProvenance dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_provenance;
    np:hasPublicationInfo dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_assertion a np:Assertion .
  
  dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_provenance a np:Provenance .
  
  dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_assertion {
  miriam-gene:9360 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN56cea779a71b77b03e48d77f80a32504 sio:SIO_000628 miriam-gene:9360, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_provenance {
  dgn-np:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_assertion dcterms:description
      "[In addition, it would be pertinent to further explore possible effects of CYP genetic variations on therapeutic and adverse outcomes of oral antidiabetics, which might be the key in optimising therapy for individual patient with Type 2 diabetes.]. 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:21108610;
    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:NP741385.RAUK4US0SI9dJ4j9Fk7JGFO6i6Jfa1MHAZbsgcDh_wCQw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:29+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" .
}