@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY> .
@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:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_head {
  this: np:hasAssertion dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion;
    np:hasProvenance dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_provenance;
    np:hasPublicationInfo dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion a np:Assertion .
  
  dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_provenance a np:Provenance .
  
  dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion {
  miriam-gene:150 a ncit:C16612 .
  
  lld:C0017178 a ncit:C7057 .
  
  dgn-gda:DGNfa8803af1a2783e43099c68fa7173884 sio:SIO_000628 miriam-gene:150, lld:C0017178;
    a sio:SIO_001122 .
}

dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_provenance {
  dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion dcterms:description
      "[ Functionally distinct alpha(2A) and alpha(2C) adrenoceptor and serotonin transporter polymorphisms are associated with constipation and high somatic symptoms in patients with lower functional gastrointestinal disorders, although the strength of the genetic contribution to the phenotype is unclear.]. 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:15138209;
    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:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}