@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc> .
@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:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_head {
  this: np:hasAssertion dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_assertion;
    np:hasProvenance dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_provenance;
    np:hasPublicationInfo dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_assertion a np:Assertion .
  
  dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_provenance a np:Provenance .
  
  dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C3463824 a ncit:C7057 .
  
  dgn-gda:DGN76f9b319a515f05a2567594fc6793857 sio:SIO_000628 miriam-gene:324, lld:C3463824;
    a sio:SIO_001121 .
}

dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_provenance {
  dgn-np:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_assertion dcterms:description
      "[These data provide a cautionary note for HSC-expansion strategies through Wnt pathway activation, provide evidence that cell extrinsic factors can contribute to the development of myeloid disease, and indicate that loss of function of APC may contribute to the phenotype observed in patients with MDS and del(5q).]. 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:20197553;
    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:NP300463.RAgm-3eSpNi2qZ8k4vX6xbfOaPOcovIHYSyObvUmL4-gc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}