@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o> .
@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:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_head {
  this: np:hasAssertion dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_assertion ;
    np:hasProvenance dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_provenance ;
    np:hasPublicationInfo dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_assertion a np:Assertion .
  dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_provenance a np:Provenance .
  dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_assertion {
  miriam-gene:4313 a ncit:C16612 .
  lld:C0011849 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_provenance {
  dgn-np:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_assertion dcterms:description "[Although no significant case-control differences in frequency of associated GG(-1575)CC(-1306)TT(-790) MMP-2 promoter genotype were observed, the genotype was found to be significantly less frequent in patients with family history of psoriasis (close as well as distant), family history of diabetes and personal history of allergy (2/11 vs. 55/32, odds ratio (OR) for GGCCTT 0.11, 95% confidential interval 0.02-0.50, Pcorr = 0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP489548.RATtoggEfRjhhsABQNpbQqr5vqHRtpxqegFzuUGQiSQ9o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:52+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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