@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY> .
@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:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_head {
  this: np:hasAssertion dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_assertion ;
    np:hasProvenance dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_provenance ;
    np:hasPublicationInfo dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_provenance a np:Provenance .
  dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_assertion {
  miriam-gene:7124 a ncit:C16612 .
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dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_provenance {
  dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_assertion dcterms:description "[SNP of TNF gene showed significant association between polymorphism and development of severe sepsis and septic shock, this would help us in evaluating patients at high risk for septic shock and such patients needed to obtain a rational basis for therapy.]. 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 ;
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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 .
}
dgn-np:NP220892.RA7gWqzAmqZHDAXZgCGUZGI7ageU3o0LJAhpoSBtk9toY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:02+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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