@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ> .
@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:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_head {
  this: np:hasAssertion dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_assertion;
    np:hasProvenance dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_provenance;
    np:hasPublicationInfo dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_assertion a np:Assertion .
  
  dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_provenance a np:Provenance .
  
  dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_assertion {
  miriam-gene:7042 a ncit:C16612 .
  
  lld:C0026691 a ncit:C7057 .
  
  dgn-gda:DGN781ae45ede353783923a058f4a9ac425 sio:SIO_000628 miriam-gene:7042, lld:C0026691;
    a sio:SIO_001121 .
}

dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_provenance {
  dgn-np:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_assertion dcterms:description
      "[Genetic variants in TGFB2, TGFBR2, and SMAD3 and their haplotypes were consistently and reproducibly associated with KD susceptibility, coronary artery aneurysm formation, aortic root dilatation, and intravenous immunoglobulin treatment response in different cohorts.]. 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:21127203;
    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:NP812151.RAin_1cg7Vh_nsq4vSuisLLk_inURcfJnHf1-xVfac-sQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:18+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" .
}