@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU> .
@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:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_head {
  this: np:hasAssertion dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_assertion;
    np:hasProvenance dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_provenance;
    np:hasPublicationInfo dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_assertion a np:Assertion .
  
  dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_provenance a np:Provenance .
  
  dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_assertion {
  miriam-gene:238 a ncit:C16612 .
  
  lld:C0206180 a ncit:C7057 .
  
  dgn-gda:DGN2278c038b2ec419210b6971549455dd1 sio:SIO_000628 miriam-gene:238, lld:C0206180;
    a sio:SIO_001121 .
}

dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_provenance {
  dgn-np:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_assertion dcterms:description
      "[In a screen for variant ALK gene fusions, we identified two ALCL that were negative for NPM-ALK by reverse transcriptase-polymerase chain reaction, but were positive for cytoplasmic ALK with both polyclonal and monoclonal antibodies to the ALK tyrosine kinase domain, consistent with ALK deregulation by an alteration other than the t(2;5) Case 1 was a T-lineage nodal and cutaneous ALCL in a 52-year-old woman, and Case 2 was a T-lineage nodal ALCL in a 12-year-old girl.]. 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:10702393;
    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:NP179165.RAYci32lYMw9XJeCSjZ-F1G1ypDOYXJldb-VOjt5N3LAU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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" .
}