@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E
> .
@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:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_head
{
this:
np:hasAssertion
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion
;
np:hasProvenance
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance
;
np:hasPublicationInfo
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion
a
np:Assertion
.
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance
a
np:Provenance
.
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGNf9538a73c09163f6e5923ef88baaa912
sio:SIO_000628
miriam-gene:64127
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance
{
dgn-np:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion
dcterms:description
"[Among the subjects in our study groups, including patients with CD, UC and healthy controls, none had OCTN and CARD15 variants and very rare IBD family history was found in our patients with the percentage of 0 (0/61 with CD) and 1.3% (2/151 with 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:18756601
;
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:NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:58+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" .
}