@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA> .
@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:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_head {
  this: np:hasAssertion dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion;
    np:hasProvenance dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_provenance;
    np:hasPublicationInfo dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion a np:Assertion .
  
  dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_provenance a np:Provenance .
  
  dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0205698 a ncit:C7057 .
  
  dgn-gda:DGNfafc483644167d3e7b19935c3501c469 sio:SIO_000628 miriam-gene:1956, lld:C0205698;
    a sio:SIO_001121 .
}

dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_provenance {
  dgn-np:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_assertion dcterms:description
      "[EFGR mutations, including 12 cases of EGFR exon 19 deletion and 11 cases of exon 21 point mutation, were present in 21 patients with adenocarcinomas, one with squamous cell carcinoma, and one with undifferentiated carcinoma.]. 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:22006985;
    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:NP701433.RAg6S4x9WimtuB48b323ngUMfTzBK5B4YeX7cNoSstkKA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:06+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" .
}