@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE
> .
@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:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_head
{
this:
np:hasAssertion
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_assertion
;
np:hasProvenance
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_provenance
;
np:hasPublicationInfo
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_assertion
a
np:Assertion
.
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_provenance
a
np:Provenance
.
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_assertion
{
miriam-gene:3553
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN628d9eeb69ab9071b3a820b4117b1c64
sio:SIO_000628
miriam-gene:3553
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_provenance
{
dgn-np:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_assertion
dcterms:description
"[The aim of this study was to determine the association of polymorphisms in the CARD15, TNFA, IL1B, and IL1RN genes with risk of development of CD and with the clinicopathological profile of CD patients.]. 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:15803022
;
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:NP699674.RA-3H9QdpF0tqXN_T-Z8goLm9125goT84fbhjMap5hBaE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}