@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4> .
@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:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_head {
  this: np:hasAssertion dgn-np:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_assertion ;
    np:hasProvenance dgn-np:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_provenance ;
    np:hasPublicationInfo dgn-np:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_assertion {
  miriam-gene:7048 a ncit:C16612 .
  lld:C0016470 a ncit:C7057 .
  dgn-gda:DGNea79903e239ee7c14be5bd4e6fcc4194 sio:SIO_000628 miriam-gene:7048 , lld:C0016470 ;
    a sio:SIO_001121 .
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dgn-np:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_provenance {
  dgn-np:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_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 ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP766673.RA6ancyqgvhAg-D_VBcsSTe8CmBI3LM5kD4JeyKIE3lW4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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