@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U> .
@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:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_head {
  this: np:hasAssertion dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_assertion;
    np:hasProvenance dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_provenance;
    np:hasPublicationInfo dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_assertion a np:Assertion .
  
  dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_provenance a np:Provenance .
  
  dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_assertion {
  miriam-gene:7043 a ncit:C16612 .
  
  lld:C0810364 a ncit:C7057 .
  
  dgn-gda:DGN3412697b9a030e255f0df6538236c1c5 sio:SIO_000628 miriam-gene:7043, lld:C0810364;
    a sio:SIO_001122 .
}

dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_provenance {
  dgn-np:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_assertion dcterms:description
      "[There was little evidence of heterogeneity in the role of TGFbeta3 between different types of oral clefts, but MSX1 did yield marginal evidence for such heterogeneity. MSX1 also showed evidence for interaction between infant's genotype and maternal smoking, giving a likelihood ratio test for heterogeneity between smoker and non-smoker mothers of 7.16 (2 df, P = 0.03). Using a conditional logistic model to test for gene-gene interaction showed no evidence of interaction between TGFbeta3 and MSX1, with both seeming to contribute independently to risk of isolated, non-syndromic oral clefts.]. 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:11754469;
    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:NP50571.RASXqaMFYHLWnUmPDWxfbBM_s7RfO872K0PsjsWflqw2U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}