@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI> .
@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:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_head {
  this: np:hasAssertion dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_assertion ;
    np:hasProvenance dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_provenance ;
    np:hasPublicationInfo dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_assertion a np:Assertion .
  dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_provenance a np:Provenance .
  dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_assertion {
  miriam-gene:3043 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
  dgn-gda:DGN8d63a15a551bfe83b626eb80abea1105 sio:SIO_000628 miriam-gene:3043 , lld:C0038454 ;
    a sio:SIO_001121 .
}
dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_provenance {
  dgn-np:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_assertion dcterms:description "[Research on the first genetic modulators of SCD, such as coinheritance of α-thalassemia and haplotypes in the β-globin gene cluster, have been followed by studies associating single nucleotide polymorphisms (SNPs) with variable risks for stroke, leg ulceration, pulmonary hypertension, priapism and osteonecrosis, with differences in the response to hydroxyurea, and with variability in the management of pain.]. 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:21083035 ;
    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:NP852919.RAksAodpBZ5UpLUTJATMnouCU5EId-mNefFrhie1tuRKI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:11+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" .
}