@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU> .
@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:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_head {
  this: np:hasAssertion dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_assertion ;
    np:hasProvenance dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_provenance ;
    np:hasPublicationInfo dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_assertion a np:Assertion .
  dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_provenance a np:Provenance .
  dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_assertion {
  miriam-gene:4313 a ncit:C16612 .
  lld:C0033860 a ncit:C7057 .
  dgn-gda:DGN9c33e0234c54f171aeaaa5984310f291 sio:SIO_000628 miriam-gene:4313 , lld:C0033860 ;
    a sio:SIO_001121 .
}
dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_provenance {
  dgn-np:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_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 ;
    sio:SIO_000772 miriam-pubmed:19360430 ;
    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:NP832565.RAhpGg2zp7T7hYYiZ4CY9I6IeSpplVPDbIEeME5Th6vtU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:29+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" .
}