@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I> .
@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:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_head {
  this: np:hasAssertion dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_assertion;
    np:hasProvenance dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_provenance;
    np:hasPublicationInfo dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_assertion a np:Assertion .
  
  dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_provenance a np:Provenance .
  
  dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_assertion {
  miriam-gene:3039 a ncit:C16612 .
  
  lld:C0271990 a ncit:C7057 .
  
  dgn-gda:DGN8425db42e11f7b70c69c6d37877377a3 sio:SIO_000628 miriam-gene:3039, lld:C0271990;
    a sio:SIO_001121 .
}

dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_provenance {
  dgn-np:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_assertion dcterms:description
      "[We selected 18 heterozygotes with the hematological phenotype of normal HbA2 (type 2) beta thalassemia who were negative for the delta beta Corfu mutation, and screened them for previously defined Mediterranean beta-thalassemia and delta-thalassemia mutations.]. 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:8034555;
    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:NP622238.RAyGr68Ua_sRAVkb2C497KN_safQu1XyCOj19vEMCiD2I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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" .
}