@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" .
}