@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o> .
@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:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_head {
  this: np:hasAssertion dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_assertion ;
    np:hasProvenance dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_provenance ;
    np:hasPublicationInfo dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_assertion a np:Assertion .
  dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_provenance a np:Provenance .
  dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_assertion {
  miriam-gene:6532 a ncit:C16612 .
  lld:C0338480 a ncit:C7057 .
  dgn-gda:DGN75d9fc7d84deb24ce428ee0a085acc66 sio:SIO_000628 miriam-gene:6532 , lld:C0338480 ;
    a sio:SIO_001121 .
}
dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_provenance {
  dgn-np:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_assertion dcterms:description "[Allelic variation of the human serotonin transporter gene (HSERT), a highly plausible candidate gene for susceptibility to migraine, was investigated in 266 individuals with migraine, including 173 having migraine without aura (MO), 94 having migraine with aura (MA), 18 with co-occurrence of MO and MA, plus 133 unaffected controls.]. 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:9601620 ;
    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:NP818302.RA8sVm9A9E54Xtp1_x0t6jdiN8qfI-n1P9QQymRBQfF_o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:21+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" .
}