@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk
> .
@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:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_head
{
this:
np:hasAssertion
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_assertion
;
np:hasProvenance
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_assertion
a
np:Assertion
.
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_provenance
a
np:Provenance
.
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_assertion
{
miriam-gene:31
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGN4fb3eb56224eb61ec267f0d637bba154
sio:SIO_000628
miriam-gene:31
,
lld:C0021390
;
a
sio:SIO_001121
.
}
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_provenance
{
dgn-np:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_assertion
dcterms:description
"[The TLR5 risk haplotype (ACC) without the two associated TLR4 SNP alleles was significantly associated with IBD, however the presence of the two TLR4 SNP risk alleles without the TLR5 risk haplotype was not statistically associated with IBD.]. 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:21203467
;
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:NP893641.RACiagzK7XlhCinKY8E-BJe3SGsq3cu57RqACEWuExyvk130_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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}