@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs> .
@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:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_head {
  this: np:hasAssertion dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_assertion ;
    np:hasProvenance dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_provenance ;
    np:hasPublicationInfo dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  lld:C0020474 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_provenance {
  dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_assertion dcterms:description "[As the SHR strain manifests many of the defining features of human metabolic Syndrome X, in which hypertension associates with insulin resistance, dyslipidaemia and abdominal obesity, the identification of genes for defective insulin and catecholamine action in SHR may facilitate gene identification in this syndrome and in related human conditions, such as type-2 diabetes and familial combined hyperlipidaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  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 ;
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dgn-np:NP333335.RAd5P62LfE6f6-biaYjVZX8hJ-dPV6N82ROMk45J6ipjs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:16+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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