@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE
> .
@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:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_head
{
this:
np:hasAssertion
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_assertion
;
np:hasProvenance
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_assertion
a
np:Assertion
.
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_provenance
a
np:Provenance
.
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_assertion
{
miriam-gene:50941
a
ncit:C16612
.
lld:C0341332
a
ncit:C7057
.
dgn-gda:DGN60df6080f24ad103633ad808b02417a1
sio:SIO_000628
miriam-gene:50941
,
lld:C0341332
;
a
sio:SIO_001121
.
}
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_provenance
{
dgn-np:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_assertion
dcterms:description
"[These OCTN1/2 variants and IBD5 marker single nucleotide polymorphisms (SNPs) (IGR2096a_1, IGR2198a_1, and IGR2230a_1) were examined in 299 Scottish children (200 with CD, 74 with ulcerative colitis (UC), and 25 with indeterminate colitis (IC)), together with 502 parents (for transmission disequilibrium testing) and 256 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:16469794
;
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:NP273893.RAl8VouKDtlK8en1uL41LW5YmTEK4-5y76xPDEdfEPlGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}