@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_head {
  this: np:hasAssertion dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_assertion ;
    np:hasProvenance dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_provenance ;
    np:hasPublicationInfo dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_assertion a np:Assertion .
  dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_provenance a np:Provenance .
  dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_assertion {
  miriam-gene:8829 a ncit:C16612 .
  lld:C0024899 a ncit:C7057 .
  dgn-gda:DGNced74d01e45aad38d0464cd73503bb59 sio:SIO_000628 miriam-gene:8829 , lld:C0024899 ;
    a sio:SIO_001122 .
}
dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_provenance {
  dgn-np:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_assertion dcterms:description "[Most patients with mastocytosis exhibit the D816V point mutation in the tyrosine kinase domain of the transmembrane receptor protein Kit, leading to its constitutive activation in bone marrow or lesional skin tissue.]. 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:16931579 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP806814.RACu18F9cjG1jX58RcKj_e7JSlG4LjAGrl4rUylmsmeI4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:48+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}