@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY
> .
@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 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:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_head
{
this:
np:hasAssertion
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion
;
np:hasProvenance
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_provenance
;
np:hasPublicationInfo
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion
a
np:Assertion
.
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_provenance
a
np:Provenance
.
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion
{
miriam-gene:3553
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGNe2662c227dfaa178dfa2165c63e4d70e
sio:SIO_000628
miriam-gene:3553
,
lld:C0007570
;
a
sio:SIO_001122
.
}
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_provenance
{
dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion
dcterms:description
"[The association between IL-10 genotypes and both histological severity at diagnosis and age of onset could be related to an alteration in cytokine balance, and supports the idea that the various clinical manifestations of the disease could be determined by a different genetic background.]. 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:16540751
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}