@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_head {
  this: np:hasAssertion dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_assertion;
    np:hasProvenance dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_provenance;
    np:hasPublicationInfo dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_assertion a np:Assertion .
  
  dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_provenance a np:Provenance .
  
  dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_assertion {
  miriam-gene:207 a ncit:C16612 .
  
  lld:C2145472 a ncit:C7057 .
  
  dgn-gda:DGN7d504c2987885e6e7dbe8739d79a4c8e sio:SIO_000628 miriam-gene:207, lld:C2145472;
    a sio:SIO_001121 .
}

dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_provenance {
  dgn-np:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_assertion dcterms:description
      "[The relative frequency at which helical domain and kinase domain mutations are found in UC is related to their potency in inducing signaling downstream of AKT and to the phenotypic effects induced in this cell type (E545K&gt;E542K&gt;H1047R).]. 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:22430209;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP968921.RAjnDBMP2uOB0sgHacFTGihvnKB2ikhhlc7JPuqhMiv80130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:04+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}