@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o> .
@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:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_head {
  this: np:hasAssertion dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion;
    np:hasProvenance dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_provenance;
    np:hasPublicationInfo dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion a np:Assertion .
  
  dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_provenance a np:Provenance .
  
  dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion {
  miriam-gene:89866 a ncit:C16612 .
  
  lld:C0028754 a ncit:C7057 .
  
  dgn-gda:DGN6821cbd36982e9289c40c725755d5d37 sio:SIO_000628 miriam-gene:89866, lld:C0028754;
    a sio:SIO_001122 .
}

dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_provenance {
  dgn-np:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_assertion dct:description
      "[The results demonstrated that genetic variation in KCNJ11, BDNF, PFKP, PTER and SEC16B were associated with SGA and support the concept that genetic factors associated with obesity and/or type 2 diabetes are more prevalent in those born SGA compared to those born AGA. We have previously determined that environmental factors are associated with differences in birthweight in the ABC study and now we have demonstrated a significant genetic contribution, suggesting that the interaction between genetics and the environment are important.]. 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:20712903;
    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:NP70381.RAQFRdWADHDiPYAxAi5Jt7vwZsNkep6GA4Cgsy1Gx-W2o130_publicationInfo {
  this: dct:created "2014-10-02T12:32:34+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" .
}