@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP642055.RA39TdyMPpwpiKntCsm3EjWhHynFPRSq9JPLFClIRN_u8> .
@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#> .
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   this: np:hasAssertion dgn-np:NP642055.RA39TdyMPpwpiKntCsm3EjWhHynFPRSq9JPLFClIRN_u8130_assertion ;
    np:hasProvenance dgn-np:NP642055.RA39TdyMPpwpiKntCsm3EjWhHynFPRSq9JPLFClIRN_u8130_provenance ;
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    a np:Nanopublication .
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dgn-np:NP642055.RA39TdyMPpwpiKntCsm3EjWhHynFPRSq9JPLFClIRN_u8130_assertion {
   miriam-gene:846 a ncit:C16612 .
  lld:C0022658 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP642055.RA39TdyMPpwpiKntCsm3EjWhHynFPRSq9JPLFClIRN_u8130_provenance {
   dgn-np:NP642055.RA39TdyMPpwpiKntCsm3EjWhHynFPRSq9JPLFClIRN_u8130_assertion dcterms:description "[In this review, data obtained in nine experimental rat models, including the Buffalo (BUF), Dahl salt-sensitive (SS), Fawn-hooded hypertensive (FHH), Goto-Kakizaki (GK), Lyon hypertensive (LH), Munich Wistar Frömter (MWF), Sabra hypertension-prone (SBH), spontaneously hypertensive rat (SHR) and stroke-prone spontaneously hypertensive rat (SHRSP) inbred strains, that contributed to the genetic dissection of renal disease phenotypes are presented.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP642055.RA39TdyMPpwpiKntCsm3EjWhHynFPRSq9JPLFClIRN_u8130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:27+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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