@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s
> .
@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:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_head
{
this:
np:hasAssertion
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_assertion
;
np:hasProvenance
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_provenance
;
np:hasPublicationInfo
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_assertion
a
np:Assertion
.
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_provenance
a
np:Provenance
.
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_assertion
{
miriam-gene:1913
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN5c08654530895496a0d3f636f12f867f
sio:SIO_000628
miriam-gene:1913
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_provenance
{
dgn-np:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_assertion
dcterms:description
"[The terminal ileum is the key site of EEC expression but detailed assessment of their subtypes, lineage transcription factors and expression products has not been undertaken in terminal ileal Crohn's disease.]. 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:22398079
;
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:NP760282.RAHJ7lj_40AVSfH_OMN0Iu4AnZkgWF_E7U-C79T9hJC6s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}