@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU> .
@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:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_head {
  this: np:hasAssertion dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_assertion;
    np:hasProvenance dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_provenance;
    np:hasPublicationInfo dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_assertion a np:Assertion .
  
  dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_provenance a np:Provenance .
  
  dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_assertion {
  miriam-gene:6927 a ncit:C16612 .
  
  lld:C0311277 a ncit:C7057 .
  
  dgn-gda:DGNb813181a654e1a93b9f7888aeaff530f sio:SIO_000628 miriam-gene:6927, lld:C0311277;
    a sio:SIO_001121 .
}

dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_provenance {
  dgn-np:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_assertion dcterms:description
      "[Analysis of statistically similar SNPs suggested that the causative variants for systolic blood pressure were located in F11R, whilst those for central obesity could be due to causative variants in the transcription factor 1 gene immediately upstream.]. 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:18067551;
    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:NP254632.RA5IobbdXAy99QD5bF1Y34ByzBmKn7ND57TWWshfrHxNU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:22+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" .
}