@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI
> .
@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:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_head
{
this:
np:hasAssertion
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_assertion
;
np:hasProvenance
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_provenance
;
np:hasPublicationInfo
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_assertion
a
np:Assertion
.
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_provenance
a
np:Provenance
.
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C1559271
a
ncit:C7057
.
dgn-gda:DGNdc6d2bf2fb9483e9737dcc53cb5a7239
sio:SIO_000628
miriam-gene:64127
,
lld:C1559271
;
a
sio:SIO_001121
.
}
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_provenance
{
dgn-np:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_assertion
dcterms:description
"[Analogous to NOD2 risk variants, TLR2 polymorphisms indicate increased susceptibility toward SBP in cirrhotic patients with ascites, and the combination of the TLR2 GT microsatellite polymorphism with at least one NOD2 risk variant enables improved identification of patients with a high risk for SBP.]. 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:21356257
;
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:NP277514.RA3Np2ty2YWJIJxVHeVRTlvzfO-034V6wR0PR8yj2sNtI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:36+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" .
}