@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y> .
@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:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_head {
  this: np:hasAssertion dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_assertion;
    np:hasProvenance dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_provenance;
    np:hasPublicationInfo dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_assertion a np:Assertion .
  
  dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_provenance a np:Provenance .
  
  dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_assertion {
  miriam-gene:2548 a ncit:C16612 .
  
  lld:C0162872 a ncit:C7057 .
  
  dgn-gda:DGN1477650dd4b887d040fbbc59eadd41de sio:SIO_000628 miriam-gene:2548, lld:C0162872;
    a sio:SIO_001121 .
}

dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_provenance {
  dgn-np:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_assertion dcterms:description
      "[A nonsense mutation was identified at codon 526 (GAA to TAA, glutamine to termination) in two cell lines (UMSCC22A and UMSCC22B) derived from the primary tumor and lymph node metastasis of the same patient.]. 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:8653689;
    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:NP1351350.RAQ0BkpGiX-EAMYCL8PfVZJu5L6XLxrbXHqPmwbpg2Z9Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:58+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" .
}