@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg> .
@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:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_head {
  this: np:hasAssertion dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_assertion ;
    np:hasProvenance dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_provenance ;
    np:hasPublicationInfo dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_assertion a np:Assertion .
  dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_provenance a np:Provenance .
  dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_assertion {
  miriam-gene:25939 a ncit:C16612 .
  lld:C1456873 a ncit:C7057 .
  dgn-gda:DGN19ee54f9aa295fdab2fd9b8a81a7dd3a sio:SIO_000628 miriam-gene:25939 , lld:C1456873 ;
    a sio:SIO_001121 .
}
dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_provenance {
  dgn-np:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_assertion dcterms:description "[After blood collection, all samples were screened for thalassemia by initial screening with the OF and DCIP tests and additional testing by CBC, RBC indices, hemoglobin typing and determination of Hb A2 and Hb E. All common alpha-thalassemia mutations were determined using the PCR with allele specific primers and Gap PCR for common deletions.]. 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:22934458 ;
    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:NP602607.RAQNYMqrnzt-mF_NweRMecIRTT9ZIa7BE8cX3UB7bIjGg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:02+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" .
}