@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4> .
@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:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_head {
  this: np:hasAssertion dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_assertion;
    np:hasProvenance dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_provenance;
    np:hasPublicationInfo dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_assertion a np:Assertion .
  
  dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_provenance a np:Provenance .
  
  dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_assertion {
  miriam-gene:10800 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGNecd4828df4adf6b8480dc8cb3b356c05 sio:SIO_000628 miriam-gene:10800, lld:C0004096;
    a sio:SIO_001122 .
}

dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_provenance {
  dgn-np:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_assertion dcterms:description
      "[To date, there has been no evidence about the expression of different splice variants of CysLT1 in asthma and their association with CYSLTR1 promoter polymorphisms.The goal of our study was to investigate CysLT1 alternative transcripts expression in asthmatic patients with different CYSLTR1 promoter haplotypes.The study groups consisted of 44 patients with asthma, diagnosed according to GINA 2008 criteria and 18 healthy subjects.]. 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:20003473;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP45611.RAW-2kG2-m2-EuNxDz0f5zZSis__u9mmTkEfF0UunpCN4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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: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" .
}