@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI
> .
@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:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_head
{
this:
np:hasAssertion
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_assertion
;
np:hasProvenance
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_assertion
a
np:Assertion
.
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_provenance
a
np:Provenance
.
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_assertion
{
miriam-gene:671
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN8ee5b390b6fcc69ea12b300980939bd2
sio:SIO_000628
miriam-gene:671
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_provenance
{
dgn-np:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_assertion
dcterms:description
"[Herein, two mutations of the Toll-like receptor (TLR)-4 gene (Asp299Gly and Thr399Ile) resulting in impaired lipopolysaccharide signaling, the -159C/T promotor polymorphism of the CD14 gene, polymorphisms of the lipopolysaccharide binding protein gene and the bactericidal permeability increasing protein gene were evaluated in 102 patients with Crohn's disease, 98 patients with ulcerative colitis and 145 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:15207785
;
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:NP934706.RAUo_crIeG5qhadyFRQNMbKDnZqDzK9TAFzDWhziODXMI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:33+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" .
}