@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw
> .
@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:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_head
{
this:
np:hasAssertion
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_assertion
;
np:hasProvenance
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_provenance
;
np:hasPublicationInfo
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_assertion
a
np:Assertion
.
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_provenance
a
np:Provenance
.
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0030193
a
ncit:C7057
.
dgn-gda:DGN17c61e85a039ec23b85817190a43222f
sio:SIO_000628
miriam-gene:1312
,
lld:C0030193
;
a
sio:SIO_001121
.
}
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_provenance
{
dgn-np:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_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:NP729891.RAx5E_I9PdA6v4YA2sc3rVsBtFxbKXRipghI9_pGOI0hw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}