@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA> .
@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/v3.0.0/void/> .

dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_head {
  this: np:hasAssertion dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_assertion;
    np:hasProvenance dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_provenance;
    np:hasPublicationInfo dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_assertion a np:Assertion .
  
  dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_provenance a np:Provenance .
  
  dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_assertion {
  miriam-gene:207 a ncit:C16612 .
  
  lld:C0007138 a ncit:C7057 .
  
  dgn-gda:DGN6eead4753b2dcb1f4dcaebe219f47ba4 sio:SIO_000628 miriam-gene:207, lld:C0007138;
    a sio:SIO_001121 .
}

dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_provenance {
  dgn-np:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP231935.RA0_bb1m2M_hN6BBY85Zdueaxbevm2CpOBJoe2qW6vlLA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:52+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}