@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI
> .
@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:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_head
{
this:
np:hasAssertion
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_assertion
;
np:hasProvenance
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_provenance
;
np:hasPublicationInfo
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_assertion
a
np:Assertion
.
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_provenance
a
np:Provenance
.
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_assertion
{
miriam-gene:7182
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGNdb73c373b14df3800a5df5cdba81309d
sio:SIO_000628
miriam-gene:7182
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_provenance
{
dgn-np:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_assertion
dcterms:description
"[MDP-induced tolerance was independent of receptor downregulation but was associated with reduced levels of phosphorylated TAK1 and abrogated phosphorylation of the downstream MAPK.Since Nod2 mutations have been associated with susceptibility to develop Crohn's disease (CD), we compared the MDP-induced tolerance in healthy donors and CD patients with compound heterozygous Nod2 mutations (Mut-Nod2) expressing variant NOD2 proteins.]. 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:19572373
;
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:NP894242.RAd8VIdAqpac5REak-eMseD2ZKFFqiRLehQEKqk3RXbzI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}