@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY
> .
@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:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_head
{
this:
np:hasAssertion
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_assertion
;
np:hasProvenance
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_provenance
;
np:hasPublicationInfo
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_assertion
a
np:Assertion
.
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_provenance
a
np:Provenance
.
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_assertion
{
miriam-gene:7097
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN7451625d13daa4e71204253b1d70f337
sio:SIO_000628
miriam-gene:7097
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_provenance
{
dgn-np:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_assertion
dcterms:description
"[Overall, no heterozygous or homozygous single nucleotide polymorphism mutations were found in patients with Crohn's disease and ulcerative colitis both in the TLR4 gene Asp299Gly, Thr399Ile and the TLR2 gene Arg677Trp, Arg753Gln in the Zhuang population from the Guangxi Zhuang Autonomous Region of China.]. 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:23239925
;
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:NP813127.RAVbcBQhgylvhiUBdm0eHjW8X0rdRZknjc1TOsS9HNwMY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}