@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ> .
@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:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_head {
  this: np:hasAssertion dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_assertion;
    np:hasProvenance dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_assertion a np:Assertion .
  
  dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_provenance a np:Provenance .
  
  dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_assertion {
  miriam-gene:5777 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGN00e055122584c1e8f9d6c402537b6205 sio:SIO_000628 miriam-gene:5777, lld:C0024299;
    a sio:SIO_001121 .
}

dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_provenance {
  dgn-np:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_assertion dcterms:description
      "[High-frequent silencing of hematopoietic cell-specific protein-tyrosine phosphatase SHP1 gene by promoter methylation was detected in various kinds of leukemias and lymphomas, as well as in many hematopoietic cell lines, which is supported by our previous observation of strong decrease of SHP1 mRNA and protein.]. 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:12438221;
    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:NP217123.RAi4OgWYEbLjiDkWWXYcaTees5o-GR2cxLoz1MQrGkPUQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}