@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc
> .
@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:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_head
{
this:
np:hasAssertion
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_assertion
;
np:hasProvenance
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_provenance
;
np:hasPublicationInfo
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_assertion
a
np:Assertion
.
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_provenance
a
np:Provenance
.
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0596240
a
ncit:C7057
.
dgn-gda:DGNceb3e2767104247bed383fea7fec1960
sio:SIO_000628
miriam-gene:1312
,
lld:C0596240
;
a
sio:SIO_001121
.
}
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_provenance
{
dgn-np:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_assertion
dcterms:description
"[Genetic variation in the COMT gene has been implicated in variable response to various experimental painful stimuli, variable susceptibility to develop common pain conditions, as well as the variable need for opioids in the treatment of cancer pain.]. 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:19374521
;
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:NP893233.RAPjAYMx5_nvJUUQI1aPkul977MwBZSNgszwXZsPspnwc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}