@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M
> .
@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:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_head
{
this:
np:hasAssertion
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion
;
np:hasProvenance
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_provenance
;
np:hasPublicationInfo
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion
a
np:Assertion
.
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_provenance
a
np:Provenance
.
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion
{
miriam-gene:1672
a
ncit:C16612
.
lld:C1719672
a
ncit:C7057
.
dgn-gda:DGN803c71629d063f4ff29d697ef7e93254
sio:SIO_000628
miriam-gene:1672
,
lld:C1719672
;
a
sio:SIO_001121
.
}
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_provenance
{
dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion
dcterms:description
"[The present case-control study was designed to investigate whether DEFB1 genomic variations are associated with the susceptibility to and the outcome of severe sepsis in 211 patients with severe sepsis and 157 ethnic-matched healthy controls.]. 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:17508030
;
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:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}