@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw> .
@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/v3.0.0/void/> .
dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_head {
  this: np:hasAssertion dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_assertion ;
    np:hasProvenance dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_provenance ;
    np:hasPublicationInfo dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_assertion a np:Assertion .
  dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_provenance a np:Provenance .
  dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGN5a2c441524c069e0e7318f66834eb0f5 sio:SIO_000628 miriam-gene:3356 , lld:C0004096 ;
    a sio:SIO_001122 .
}
dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_provenance {
  dgn-np:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_assertion dcterms:description "[ We have explored the frequencies of important allelic variants DCP1, CETP, ADRB2, and HTR2A among the Egyptian population focusing on the ethnic diversity in the distribution of the tested mutant alleles. Our results may help in better understanding the ]. 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:11956670 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP73161.RAs_3_amLFQQw7KCj_svIJaxWv84gomcEx7giXTheCllw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:20+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}