@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY> .
@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:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_head {
  this: np:hasAssertion dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion;
    np:hasProvenance dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_provenance;
    np:hasPublicationInfo dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion a np:Assertion .
  
  dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_provenance a np:Provenance .
  
  dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C2939461 a ncit:C7057 .
  
  dgn-gda:DGN45dab556ebd733db0accf88809983ad4 sio:SIO_000628 miriam-gene:861, lld:C2939461;
    a sio:SIO_001121 .
}

dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_provenance {
  dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion dcterms:description
      "[Abstract Familial platelet disorder with predisposition to acute myeloid leukemia (FPD/AML) is an autosomal dominant disorder characterized by mild to moderate thrombocytopenia with or without its impaired function, inherited RUNX1 mutation and high incidence of myeloid malignancy, such as myelodysplastic syndrome or acute myeloid leukemia.]. 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:23971860;
    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:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:23+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" .
}