@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64> .
@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:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_head {
  this: np:hasAssertion dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_assertion;
    np:hasProvenance dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_provenance;
    np:hasPublicationInfo dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_assertion a np:Assertion .
  
  dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_provenance a np:Provenance .
  
  dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_assertion {
  miriam-gene:26191 a ncit:C16612 .
  
  lld:C0221013 a ncit:C7057 .
  
  dgn-gda:DGN2561dc58ea5abec4dbf6f5d199844e03 sio:SIO_000628 miriam-gene:26191, lld:C0221013;
    a sio:SIO_001121 .
}

dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_provenance {
  dgn-np:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_assertion dcterms:description
      "[Here, we assessed the potential association between the immunophenotype of MC and multilineage KIT mutation in the BM of SM patients through the investigation of the flow cytometric protein expression profile (PEP) of bone marrow mast cells (BMMC) from 70 control individuals and 206 SM patients, classified according to the WHO (World Health Organization), and the degree of involvement of BM hematopoiesis by the D816V KIT mutation; additionally, we developed a score-based class prediction algorithm for the detection of SM cases with multilineage mutation.]. 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:22051531;
    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:NP208884.RAb6wMnw0MsnAiks-p2X44ULXsJIl_yUS2TDSfCZHVA64130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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" .
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