@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU> .
@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:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_head {
  this: np:hasAssertion dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_assertion;
    np:hasProvenance dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_provenance;
    np:hasPublicationInfo dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_assertion a np:Assertion .
  
  dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_provenance a np:Provenance .
  
  dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_assertion {
  miriam-gene:1144 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN5bd47c4713647c461de2f96f32ae100a sio:SIO_000628 miriam-gene:1144, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_provenance {
  dgn-np:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_assertion dcterms:description
      "[CHRNG is currently thought to be expressed only during fetal development. These findings support the Barker hypothesis, that fetal genotype and intra-uterine environment influence susceptibility to chronic diseases later in life. Additional studies of this variant in other populations, as well as the effect of this variant on acetylcholine receptor expression and function, are needed to further elucidate its potential role in the regulation of blood pressure. This study suggests for the first time in humans, a possible role for genetic variation in the neuromuscular nicotinic acetylcholine receptor, particularly the gamma subunit, in systolic blood pressure regulation.]. 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:18625075;
    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:NP90029.RAA4Jc4s68cRIdTgYSCvqczqRcMFIaDO5ROZaU6CI3bEU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:44+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" .
}