@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g> .
@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 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:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_head {
  this: np:hasAssertion dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_assertion;
    np:hasProvenance dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_provenance;
    np:hasPublicationInfo dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_assertion a np:Assertion .
  
  dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_provenance a np:Provenance .
  
  dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_assertion {
  miriam-gene:51284 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN8fa683cc85591fbe2903657cac393218 sio:SIO_000628 miriam-gene:51284, lld:C0242383;
    a sio:SIO_001122 .
}

dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_provenance {
  dgn-np:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_assertion dct:description
      "[Although borderline support for association between polymorphisms in TLR genes and AMD was reported for some cohorts, these initial observations of coding SNPs in TLR3, TLR4, and TLR7 were not replicated.]. 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:18385087;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP79055.RA4iKSzoc1WH5Fcx8xFMPuB4uOQryUjDInJ2gTq1o6I8g130_publicationInfo {
  this: dct:created "2014-10-02T12:32:39+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}