@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_head
{
this:
np:hasAssertion
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_assertion
;
np:hasProvenance
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_provenance
;
np:hasPublicationInfo
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_assertion
a
np:Assertion
.
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_provenance
a
np:Provenance
.
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN9d3f37d0f20dfd9585bb8b44f8018f05
sio:SIO_000628
miriam-gene:64127
,
lld:C0010346
;
a
sio:SIO_001122
.
}
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_provenance
{
dgn-np:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_assertion
dcterms:description
"[The second models the NOD2 3020insC SNP, which is the most common and highest risk variant in Crohn's disease, and examines the ability of food components or extracts to restore the normal phenotype in the mutant cell line.]. 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:17568627
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP615191.RAb9v_4Ck4vYw2AT6jxJD3jDgGYWmqsdY6pFX0xis80KA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:24+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}