@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE> .
@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:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_head {
  this: np:hasAssertion dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_assertion ;
    np:hasProvenance dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_provenance ;
    np:hasPublicationInfo dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_assertion a np:Assertion .
  dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_provenance a np:Provenance .
  dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  lld:C0025303 a ncit:C7057 .
  dgn-gda:DGNcf89fc5747d477fd56bd160900924353 sio:SIO_000628 miriam-gene:1636 , lld:C0025303 ;
    a sio:SIO_001121 .
}
dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_provenance {
  dgn-np:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_assertion dcterms:description "[The absence (deletion, D) rather than the presence (insertion, I) of a 287 base pair fragment in the ACE gene is associated with higher circulating and tissue ACE activity, with excess mortality in critical illness (including adult acute respiratory distress syndrome and paediatric meningococcal infection) and with worse functional outcome from traumatic brain injury.]. 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:18955615 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP616430.RAckoZ-gsVt8S8f8PXaR7mshFwbVDHhoDp1K22fkMG_iE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:12+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}