@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM
> .
@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:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_head
{
this:
np:hasAssertion
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_assertion
;
np:hasProvenance
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_provenance
;
np:hasPublicationInfo
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_assertion
a
np:Assertion
.
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_provenance
a
np:Provenance
.
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_assertion
{
miriam-gene:3704
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN396543dc5c6ae4b8432db2563a638118
sio:SIO_000628
miriam-gene:3704
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_provenance
{
dgn-np:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_assertion
dcterms:description
"[The aim of this study was to determine the frequencies of TPMT and ITPA polymorphisms in Crohn's disease patients of Tunisian origin and to compare them with allele frequencies previously reported in other populations of various ethnic origins.]. 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:22225964
;
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:NP413033.RAbChVtfop40VoXI4ruKbx2XnKypp9OcW3qHNCU2RrfoM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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
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"v2.1.0" .
}