@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw
> .
@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:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_head
{
this:
np:hasAssertion
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_assertion
;
np:hasProvenance
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_provenance
;
np:hasPublicationInfo
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_assertion
a
np:Assertion
.
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_provenance
a
np:Provenance
.
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_assertion
{
miriam-gene:5021
a
ncit:C16612
.
lld:C0022104
a
ncit:C7057
.
dgn-gda:DGNe285cf13ded67724d82807994641871e
sio:SIO_000628
miriam-gene:5021
,
lld:C0022104
;
a
sio:SIO_001122
.
}
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_provenance
{
dgn-np:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_assertion
dcterms:description
"[Genetic variants in the OXT promoter region, and in the OXTR gene in DNA samples from 131 rigorously evaluated patients with Irritable Bowel Syndrome (IBS), 408 homozygous subjects referred for lactase (LCT-13910 C>T, rs4988235) genotyping, and 299 asymptomatic blood donors were compared.]. 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:19943975
;
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:NP68579.RAJPfHjuKM5nstougu_JIItjIzB99h-F6WaP_xtbgRrhw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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" .
}