@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c
> .
@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:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_head
{
this:
np:hasAssertion
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_assertion
;
np:hasProvenance
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_assertion
a
np:Assertion
.
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_provenance
a
np:Provenance
.
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_assertion
{
miriam-gene:958
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN426ab2ac503d81e3f2491d7b77e9a8b2
sio:SIO_000628
miriam-gene:958
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_provenance
{
dgn-np:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_assertion
dcterms:description
"[We hypothesized that this functional polymorphism might also show an association with other complex autoimmune condition such as inflammatory bowel disease, given the CD40 overexpression previously observed in Crohn's disease (CD) lesions.]. 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:20634952
;
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:NP416842.RAPWC8akm6GEgclA3NkynqgsoBekKrQ1ubl0iQhK46i_c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}