@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w> .
@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:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_head {
  this: np:hasAssertion dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_assertion;
    np:hasProvenance dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_provenance;
    np:hasPublicationInfo dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_assertion a np:Assertion .
  
  dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_provenance a np:Provenance .
  
  dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_assertion {
  miriam-gene:6319 a ncit:C16612 .
  
  lld:C2939420 a ncit:C7057 .
  
  dgn-gda:DGNb22a8bed96ab8637467d3d8d5f55d1ae sio:SIO_000628 miriam-gene:6319, lld:C2939420;
    a sio:SIO_001121 .
}

dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_provenance {
  dgn-np:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_assertion dcterms:description
      "[Increased SCD1 expression supports ccRCC viability and therefore we propose it as a novel molecular target for therapy either independently or in combination with an mTOR inhibitor for patients whose disease cannot be remedied with surgical intervention, such as in cases of advanced or metastatic 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:23633458;
    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:NP786483.RA77a0QUQ12B0Y1KTHclUqejv9rFkoJth3_R325vn461w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:56+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" .
}