@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs> .
@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:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_head {
  this: np:hasAssertion dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion;
    np:hasProvenance dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_provenance;
    np:hasPublicationInfo dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion a np:Assertion .
  
  dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_provenance a np:Provenance .
  
  dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0039494 a ncit:C7057 .
  
  dgn-gda:DGNb33a2025d5ab45a6aad24a9c4ade1937 sio:SIO_000628 miriam-gene:2099, lld:C0039494;
    a sio:SIO_001121 .
}

dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_provenance {
  dgn-np:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_assertion dcterms:description
      "[The aim of this study is to identify any association between variants of the polymorphic estrogen receptor gene and various symptoms of temporomandibular disorder (TMD) including pain in the temporomandibular joint and masticatory muscles, joint crepitus, limited range of jaw movement, and bone changes in the condylar head.]. 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:20656393;
    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:NP712612.RAwdQEgRbddtnSQfRNlJou2nsBKNHsFQ1fvEnXlyLDacs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:13+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" .
}