@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA> .
@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/v4.0.0/void/> .

dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_head {
  this: np:hasAssertion dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion;
    np:hasProvenance dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_provenance;
    np:hasPublicationInfo dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion a np:Assertion .
  
  dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_provenance a np:Provenance .
  
  dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion {
  miriam-gene:2623 a ncit:C16612 .
  
  lld:C0023462 a ncit:C7057 .
  
  dgn-gda:DGN27bd1e2ea7d4acf100b0246ab7a9f353 sio:SIO_000628 miriam-gene:2623, lld:C0023462;
    a sio:SIO_001121 .
}

dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_provenance {
  dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion dcterms:description
      "[These data show GATA1 mutations occur in utero in most DS TMD and AMKL, that they may occur without clinical signs of disease, and that multiple separate GATA1 mutant clones can occur in an individual.]. 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:14656875;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:57+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}