@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8
> .
@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:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_head
{
this:
np:hasAssertion
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_assertion
;
np:hasProvenance
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_provenance
;
np:hasPublicationInfo
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_assertion
a
np:Assertion
.
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_provenance
a
np:Provenance
.
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGNf40760bc7eb6205a3fc19289e45f5574
sio:SIO_000628
miriam-gene:64127
,
lld:C0021390
;
a
sio:SIO_001121
.
}
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_provenance
{
dgn-np:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_assertion
dcterms:description
"[The identification of the role of genetic variants within NOD2 (CARD15) in Crohn's disease and ulcerative colitis susceptibility highlight the role of the innate immune system in inflammatory bowel disease (IBD) pathogenesis.]. 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:15790594
;
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:NP164292.RAF76AbhlxQfoHqHaQJoDCuusdm-nU_YjlhCt61AhF3T8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}