@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ
> .
@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:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_head
{
this:
np:hasAssertion
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_assertion
;
np:hasProvenance
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_assertion
a
np:Assertion
.
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_provenance
a
np:Provenance
.
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGN1714316991b156c85aebcfe075e59b51
sio:SIO_000628
miriam-gene:1312
,
lld:C0011570
;
a
sio:SIO_001121
.
}
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_provenance
{
dgn-np:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_assertion
dcterms:description
"[Since pain syndromes as well as anxiety and depression are associated to low and high COMT activity respectively and these conditions are all associated with irritable bowel syndrome (IBS) we wanted for the first time to explore the relationship between the polymorphism and IBS.]. 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:21437260
;
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:NP261573.RATdpVO8NAOAt8ZiAo0fyxaaeeXcaHs5SZx8qh9dMq7eQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}