@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo> .
@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:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_head {
  this: np:hasAssertion dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion;
    np:hasProvenance dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_provenance;
    np:hasPublicationInfo dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion a np:Assertion .
  
  dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_provenance a np:Provenance .
  
  dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion {
  miriam-gene:11122 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN8107dd1784f323fc695e98164f50bd06 sio:SIO_000628 miriam-gene:11122, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_provenance {
  dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion dcterms:description
      "[Contrary to the previous report on the frequent PTPTR phosphatase domain mutations in colon cancers, this study demonstrated that the somatic mutation of the PTPRT phosphatase domain rarely occurred in common human cancers.]. 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:17223850;
    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:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}