@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_head {
  this: np:hasAssertion dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_assertion;
    np:hasProvenance dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_provenance;
    np:hasPublicationInfo dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_assertion a np:Assertion .
  
  dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_provenance a np:Provenance .
  
  dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_assertion {
  miriam-gene:7046 a ncit:C16612 .
  
  lld:C2697932 a ncit:C7057 .
  
  dgn-gda:DGNccb680b73cd824e26cbd86512019dd1f sio:SIO_000628 miriam-gene:7046, lld:C2697932;
    a sio:SIO_001121 .
}

dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_provenance {
  dgn-np:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_assertion dcterms:description
      "[We demonstrate that patients with Loeys-Dietz syndrome (LDS), an autosomal dominant disorder caused by mutations in the genes encoding receptor subunits for TGFβ, TGFBR1 and TGFBR2, are strongly predisposed to develop allergic disease, including asthma, food allergy, eczema, allergic rhinitis, and eosinophilic gastrointestinal disease.]. 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:23884466;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1096564.RA12J9kHz8pr6rj6MS4iaKq1kbWBLLXzgTM9kIe_i5RNo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:03+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}