@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0
> .
@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:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_head
{
this:
np:hasAssertion
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_assertion
;
np:hasProvenance
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_provenance
;
np:hasPublicationInfo
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_assertion
a
np:Assertion
.
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_provenance
a
np:Provenance
.
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_assertion
{
miriam-gene:4049
a
ncit:C16612
.
lld:C1719672
a
ncit:C7057
.
dgn-gda:DGN961a70be2388e0b8c169d8e72f2f15a2
sio:SIO_000628
miriam-gene:4049
,
lld:C1719672
;
a
sio:SIO_001121
.
}
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_provenance
{
dgn-np:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_assertion
dcterms:description
"[Although the TNF-beta NcO1 polymorphism appears to be less likely to be causative for development of severe sepsis after trauma, it is thus far the only genetic marker identified which can be used as a relevant risk estimate for severe sepsis in trauma patients immediately after the 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:12414751
;
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:NP580173.RAhTRn2UmSuWkivnPqhL1zK037kpQFTArU8Le2hH_KOH0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}