@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8
> .
@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:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_head
{
this:
np:hasAssertion
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_assertion
;
np:hasProvenance
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_provenance
;
np:hasPublicationInfo
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_assertion
a
np:Assertion
.
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_provenance
a
np:Provenance
.
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGNcd4922f3190ecd35907341eef2b8954e
sio:SIO_000628
miriam-gene:3133
,
lld:C0021390
;
a
sio:SIO_001121
.
}
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_provenance
{
dgn-np:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_assertion
dcterms:description
"[We now have a much more detailed appreciation of the molecular genetic architecture of inflammatory bowel disease (IBD), and particularly the areas of overlap between Crohn's disease (CD) and ulcerative colitis (UC) (such as Th17 pathways) and the pathways which are disease-specific (such as NOD2 and autophagy for CD and the MHC and epithelial barrier genes for UC).]. 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:23075873
;
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:NP250743.RADVASeAoexQd2tXolIlWOEU7An1HO-Vw3RD8_iozj5I8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}