@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng
> .
@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:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_head
{
this:
np:hasAssertion
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_assertion
;
np:hasProvenance
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_provenance
;
np:hasPublicationInfo
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_assertion
a
np:Assertion
.
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_provenance
a
np:Provenance
.
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_assertion
{
miriam-gene:3596
a
ncit:C16612
.
lld:C1290884
a
ncit:C7057
.
dgn-gda:DGN7c3bacfa0b4cf91e4c73227a17dfdf54
sio:SIO_000628
miriam-gene:3596
,
lld:C1290884
;
a
sio:SIO_001121
.
}
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_provenance
{
dgn-np:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_assertion
dcterms:description
"[We have assayed genetic variation at the IL4, IL5, IL9, IL13, IL17B and NR3C1 (GR) loci, all of which are present on chromosome 5q and have potential or demonstrated involvement in autoimmune and/or inflammatory disease, in a sample of 409 CD cases and 355 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:15713213
;
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:NP667651.RAQ954hTipoF0hvIt7xDDXC2pMmIjTJpC0OpUfJfc_Dng130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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" .
}