@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU
> .
@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:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_head
{
this:
np:hasAssertion
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_assertion
;
np:hasProvenance
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_provenance
;
np:hasPublicationInfo
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_assertion
a
np:Assertion
.
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_provenance
a
np:Provenance
.
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_assertion
{
miriam-gene:6584
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN9ded176fffe277462506a96cb5ee3b17
sio:SIO_000628
miriam-gene:6584
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_provenance
{
dgn-np:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_assertion
dcterms:description
"[The aim of this study was to verify the prevalence rate of the haplotype called TC, determined by combination of two functional alleles of OCTN cation transporter genes (SLC22A4 1672T and SLC22A5 -207C combination variants) in ulcerative colitis patients and unrelated healthy controls.]. 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:17387389
;
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:NP520476.RAQik3zAxFP6lju5oHjgevDEHJUkXuOztaP3Te8_bqMxU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}