@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM> .
@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:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_head {
  this: np:hasAssertion dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_assertion;
    np:hasProvenance dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_provenance;
    np:hasPublicationInfo dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_assertion a np:Assertion .
  
  dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_provenance a np:Provenance .
  
  dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_assertion {
  miriam-gene:947 a ncit:C16612 .
  
  lld:C0019829 a ncit:C7057 .
  
  dgn-gda:DGNb891703745cd88b51c8d030b72df7684 sio:SIO_000628 miriam-gene:947, lld:C0019829;
    a sio:SIO_001121 .
}

dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_provenance {
  dgn-np:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_assertion dcterms:description
      "[The objective of the current study was to 1) identify this protein using two independent methods, 2) study the expression of the protein and its encoding mRNA in reactive lymph nodes, normal lymphocytes and CD34+ bone marrow precursor cells, 3) analyse patterns of expression of the protein in tissue microarrays assembled from a large number of diagnostic clinical biopsies from patients with HL, and 4) determine the copy number variation and mutation status of the encoding gene in HL cell lines.]. 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:20100355;
    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:NP828842.RAxuVxWPfbLQ7sA226UOMhXYAhkMbG48Dnjo0tt7GOZXM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:27+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" .
}