@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM> .
@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:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_head {
  this: np:hasAssertion dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_assertion;
    np:hasProvenance dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_provenance;
    np:hasPublicationInfo dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_assertion a np:Assertion .
  
  dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_provenance a np:Provenance .
  
  dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0206368 a ncit:C7057 .
  
  dgn-gda:DGN082adb2fda7e165a6358bfb4bb549562 sio:SIO_000628 miriam-gene:7099, lld:C0206368;
    a sio:SIO_001121 .
}

dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_provenance {
  dgn-np:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_assertion dcterms:description
      "[The allele frequency of rs2149356 of the TLR4 gene in the POAG, NTG, and XFG groups was the most significantly different from that of the control group (minor allele frequency 0.446, 0.395, 0.404, vs 0.308; P = .000058, P = .0030, and P = .015).]. 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:22831837;
    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:NP728785.RAYoblX5arp9iHwBGqvr1DC8LRGFD8OH2gi4fVa9h2MxM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:22+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" .
}