@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I
> .
@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:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_head
{
this:
np:hasAssertion
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_assertion
;
np:hasProvenance
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_provenance
;
np:hasPublicationInfo
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_assertion
a
np:Assertion
.
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_provenance
a
np:Provenance
.
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_assertion
{
miriam-gene:3586
a
ncit:C16612
.
lld:C0035222
a
ncit:C7057
.
dgn-gda:DGNfe0522c57f9604f6b773680be55f21f6
sio:SIO_000628
miriam-gene:3586
,
lld:C0035222
;
a
sio:SIO_001121
.
}
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_provenance
{
dgn-np:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_assertion
dcterms:description
"[The biallelic IL-10 single nucleotide polymorphism at -1082 of the promoter region linked to individual variation in cytokine inducibility has been strongly implicated in several pathological conditions including the development of, and outcomes in, septic shock during pneumococcal infection, acute respiratory distress syndrome, and cardiac dysfunction.]. 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:20181890
;
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:NP864275.RAspHewNtXKPEZ756q9ZU8k9FqQhacv2UNghD0yGpMV4I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}