@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I
> .
@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:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_head
{
this:
np:hasAssertion
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion
;
np:hasProvenance
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_provenance
;
np:hasPublicationInfo
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion
a
np:Assertion
.
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_provenance
a
np:Provenance
.
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion
{
miriam-gene:3558
a
ncit:C16612
.
lld:C0023895
a
ncit:C7057
.
dgn-gda:DGN651da2769d5e8624fe019b33f41d2617
sio:SIO_000628
miriam-gene:3558
,
lld:C0023895
;
a
sio:SIO_001121
.
}
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_provenance
{
dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion
dcterms:description
"[Considering the strong coincidence of primary sclerosing cholangitis (PSC) with UC and the increased frequency of other autoimmune disorders in patients with primary biliary cirrhosis (PBC), we investigated whether genetic variation in the IL2/IL21 region may also modulate the susceptibility to these two rare cholestatic liver diseases.]. 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:21304239
;
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:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:11+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" .
}