@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU> .
@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:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_head {
  this: np:hasAssertion dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion ;
    np:hasProvenance dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_provenance ;
    np:hasPublicationInfo dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion a np:Assertion .
  dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_provenance a np:Provenance .
  dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion {
  miriam-gene:8266 a ncit:C16612 .
  lld:C0017758 a ncit:C7057 .
  dgn-gda:DGN0b22f0ea5246bb24b428a96d96afd770 sio:SIO_000628 miriam-gene:8266 , lld:C0017758 ;
    a sio:SIO_001121 .
}
dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_provenance {
  dgn-np:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_assertion dcterms:description "[The frequencies of four major red cell genetic defects, sickle haemoglobin (Hb S), glucose 6 phosphate dehydrogenase deficiency (G6PD), and alpha and beta thalassaemia, have been determined in nearly 5000 subjects from the three major Peninsular Arab States, namely Yemen (North and South), the United Arab Emirates, and Oman.]. 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:3723553 ;
    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:NP428369.RA6i9H1yxWmVPOtHVEAlWb0ZDhIezSvODNMzL-R9XCiTU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:14+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" .
}