@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc> .
@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:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_head {
  this: np:hasAssertion dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion;
    np:hasProvenance dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_provenance;
    np:hasPublicationInfo dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion a np:Assertion .
  
  dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_provenance a np:Provenance .
  
  dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion {
  miriam-gene:2004 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGNebd2ae4074f1b6a6c60d5a04295f4407 sio:SIO_000628 miriam-gene:2004, lld:C1263846;
    a sio:SIO_001121 .
}

dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_provenance {
  dgn-np:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_assertion dcterms:description
      "[The norepinephrine transporter (NET, SLC6A2) represents an important candidate gene for contribution to ADHD because it regulates catecholamine extracellular and tissue concentrations and contributes to executive functions disrupted in ADHD, and NET is a target for most effective ADHD therapeutics.]. 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:19698724;
    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:NP449158.RACAf2S3OrVLFu_B_PwMevUYX7nh5K6REBWFD4MBMtSxc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:28+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" .
}