@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58> .
@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:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_head {
  this: np:hasAssertion dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_assertion;
    np:hasProvenance dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_provenance;
    np:hasPublicationInfo dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_assertion a np:Assertion .
  
  dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_provenance a np:Provenance .
  
  dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_assertion {
  miriam-gene:6584 a ncit:C16612 .
  
  lld:C0149721 a ncit:C7057 .
  
  dgn-gda:DGN705535ea5d72c60d9b8fd047703664c6 sio:SIO_000628 miriam-gene:6584, lld:C0149721;
    a sio:SIO_001122 .
}

dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_provenance {
  dgn-np:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_assertion dcterms:description
      "[ These results identify the carnitine-transporter gene family as candidate modifiers of LVMI in human hypertension. The use of common SNPs to define informative haplotypes associated with the phenotype of interest is the starting point for progress toward identification of the trapped contributing SNP(s).]. 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:15647998;
    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:NP51657.RAdQ-5OyD_3t9alj83TPa_LkgHN0nKATnxCmtqpbWEf58130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}