@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0> .
@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:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_head {
   this: np:hasAssertion dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_assertion ;
    np:hasProvenance dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_provenance ;
    np:hasPublicationInfo dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_assertion a np:Assertion .
  dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_provenance a np:Provenance .
  dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_assertion {
   miriam-gene:2993 a ncit:C16612 .
  lld:C0019045 a ncit:C7057 .
  dgn-gda:DGN8dbae69ce0e263c1090d36f588a32e6a sio:SIO_000628 miriam-gene:2993 , lld:C0019045 ;
    a sio:SIO_001121 .
}
dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_provenance {
   dgn-np:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_assertion dcterms:description "[All samples were analysed by DNA array analysis (HEA Beadchip(TM), Bioarray Solutions) to determine polymorphisms associated with antigen expression for 11 blood group systems (Rh, Kell, Kidd, Duffy, MNS, Dombrock, Lutheran, Landsteiner-Wiener, Diego, Colton, Scianna); and one mutation associated with haemoglobinopathies.]. 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:19392786 ;
    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:NP209477.RApbZZCQwRCG4eVHxFKzVu21qLrZX0fVePsdsLAshOOB0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:55+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" .
}