@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_head {
  this: np:hasAssertion dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_assertion ;
    np:hasProvenance dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_provenance ;
    np:hasPublicationInfo dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_assertion a np:Assertion .
  dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_provenance a np:Provenance .
  dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  lld:C0036396 a ncit:C7057 .
  dgn-gda:DGNaa3b8183239af03346a67a813377cf38 sio:SIO_000628 miriam-gene:1312 , lld:C0036396 ;
    a sio:SIO_001122 .
}
dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_provenance {
  dgn-np:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_assertion dcterms:description "[We examined if the COMT Val158Met SNP could contribute to discogenic subacute low back pain and sciatica by comparing the frequency of the Val158Met genotypes of degenerative disc disease patients with healthy 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:22337560 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP961093.RAUFNaOGhdQbzYxgzaWx-WPKBis_TmdcxrYoyc346YqBw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:00+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}