@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk
> .
@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:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_head
{
this:
np:hasAssertion
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion
;
np:hasProvenance
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_provenance
;
np:hasPublicationInfo
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion
a
np:Assertion
.
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_provenance
a
np:Provenance
.
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion
{
miriam-gene:7099
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN5e0f48c4e956fa32cc90f89a4a23338c
sio:SIO_000628
miriam-gene:7099
,
lld:C0009324
;
a
sio:SIO_001122
.
}
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_provenance
{
dgn-np:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_assertion
dcterms:description
"[ CARD15 polymorphisms are seen in greater frequency in patients with pouchitis after IPAA for UC. These findings, if borne out in prospective analyses, suggest that CARD15 mutations, particularly L1007fsinsC, may predispose to the development of pouchitis after IPAA for 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:16239841
;
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:NP50379.RAQuWInwqEZuibOmAjF5OEO772sOxtcCHlfPQx74usTmk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}